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dbVar

Database of genomic structural variation

esv3721

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:304

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: 154 SVs from 28 studies. See in: genome view

Remapped(Score: Perfect):202,624,790-202,625,093

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
esv3721	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	202,624,790	202,625,093
esv3721	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	202,593,918	202,594,221
esv3721	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000001.9	Chr1	200,860,541	200,860,844

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
essv26162	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
essv26162	Remapped	Perfect	GRCh38.p12	First Pass	NC_000001.11	Chr1	202,624,790	202,625,093
essv26162	Remapped	Perfect	GRCh37.p13	First Pass	NC_000001.10	Chr1	202,593,918	202,594,221
essv26162	Submitted genomic		NCBI36 (hg18)		NC_000001.9	Chr1	200,860,541	200,860,844

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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