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dbVar

Database of genomic structural variation

nsv482710

Organism: Homo sapiens

Study:nstd40 (Sharp et al. 2006)
Variant Type:sequence alteration
Method Type:BAC aCGH
Submitted on:NCBI34 (hg16)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:150,557

Publication(s):Sharp et al. 2006

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: 640 SVs from 77 studies. See in: genome view

Remapped(Score: Good):72,595,336-72,745,892

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv482710	Remapped	Good	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	72,595,336	72,745,892
nsv482710	Remapped	Pass	GRCh37.p13	Primary Assembly	Second Pass	NC_000007.13	Chr7	72,060,321	72,196,404
nsv482710	Remapped	Pass	GRCh37.p13	PATCHES	First Pass	NW_003871064.1	Chr7\|NW_00 3871064.1	124,600	260,683
nsv482710	Submitted genomic		NCBI34 (hg16)	Primary Assembly		NC_000007.10	Chr7	71,472,438	71,622,982

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv3005848	sequence alteration	BAC aCGH	Probe signal intensity

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv3005848	Remapped	Good	GRCh38.p12	First Pass	NC_000007.14	Chr7	72,595,336	72,745,892
nssv3005848	Remapped	Pass	GRCh37.p13	First Pass	NW_003871064.1	Chr7\|NW_00 3871064.1	124,600	260,683
nssv3005848	Remapped	Pass	GRCh37.p13	Second Pass	NC_000007.13	Chr7	72,060,321	72,196,404
nssv3005848	Submitted genomic		NCBI34 (hg16)		NC_000007.10	Chr7	71,472,438	71,622,982

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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