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dbVar

Database of genomic structural variation

esv4732

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:753

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: 133 SVs from 33 studies. See in: genome view

Remapped(Score: Perfect):52,524,041-52,524,793

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
esv4732	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000015.10	Chr15	52,524,041	52,524,793
esv4732	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	52,816,238	52,816,990
esv4732	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000015.8	Chr15	50,603,530	50,604,282

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
essv27173	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
essv27173	Remapped	Perfect	GRCh38.p12	First Pass	NC_000015.10	Chr15	52,524,041	52,524,793
essv27173	Remapped	Perfect	GRCh37.p13	First Pass	NC_000015.9	Chr15	52,816,238	52,816,990
essv27173	Submitted genomic		NCBI36 (hg18)		NC_000015.8	Chr15	50,603,530	50,604,282

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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