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dbVar

Database of genomic structural variation

esv3797786

Organism: Homo sapiens

Study:estd192 (COSMIC)
Variant Type:complex chromosomal rearrangement
Method Type:Curated
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:401

Description:Chr8:g.(37568619_37569019)_chr8:o(129449661_12
9450061)bkpt
Publication(s):Forbes et al. 2008, Forbes et al. 2008, Stephens et al. 2009

Links to Other Resources

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 136 SVs from 15 studies. See in: genome view

Remapped(Score: Perfect):37,711,101-37,711,501

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop	strand
esv3797786	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	37,711,101	37,711,501	37,711,101	37,711,501
esv3797786	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	128,437,415	128,437,815	128,437,415	128,437,815	-
esv3797786	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000008.10	Chr8	37,568,619	37,569,019	37,568,619	37,569,019
esv3797786	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000008.10	Chr8	129,449,661	129,450,061	129,449,661	129,450,061	-

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
essv16625634	intrachromosomal translocation	1126512	Curated	Curated	111

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop	strand
essv16625634	Remapped	Perfect	GRCh38.p12	First Pass	NC_000008.11	Chr8	37,711,101	37,711,501	37,711,101	37,711,501	not reported
essv16625634	Remapped	Perfect	GRCh38.p12	First Pass	NC_000008.11	Chr8	128,437,415	128,437,815	128,437,415	128,437,815	-
essv16625634	Submitted genomic		GRCh37 (hg19)		NC_000008.10	Chr8	37,568,619	37,569,019	37,568,619	37,569,019	not reported
essv16625634	Submitted genomic		GRCh37 (hg19)		NC_000008.10	Chr8	129,449,661	129,450,061	129,449,661	129,450,061	-

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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