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dbVar

Database of genomic structural variation

esv5115

Organism: Homo sapiens

Study:estd3 (Wang et al. 2008)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:NCBI36 (hg18)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:201

Publication(s):Wang et al. 2008

Links to Other Resources

Overlapping Genes

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: 216 SVs from 35 studies. See in: genome view

Remapped(Score: Perfect):108,973-109,173

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
esv5115	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000018.10	Chr18	108,973	109,173
esv5115	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	108,973	109,173
esv5115	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000018.8	Chr18	98,973	99,173

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
essv27556	complex substitution	YH	Sequencing	Read depth and paired-end mapping	2,682

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
essv27556	Remapped	Perfect	GRCh38.p12	First Pass	NC_000018.10	Chr18	108,973	109,173
essv27556	Remapped	Perfect	GRCh37.p13	First Pass	NC_000018.9	Chr18	108,973	109,173
essv27556	Submitted genomic		NCBI36 (hg18)		NC_000018.8	Chr18	98,973	99,173

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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