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dbVar

Database of genomic structural variation

nsv499086

Organism: Homo sapiens

Study:nstd47 (Kidd et al. 2010b)
Variant Type:inversion
Method Type:Sequencing
Submitted on:NCBI36 (hg18)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:39,486

Publication(s):Kidd et al. 2010

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: 215 SVs from 48 studies. See in: genome view

Remapped(Score: Perfect):48,866,456-48,905,941

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv499086	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	48,866,456	48,905,941
nsv499086	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	48,906,052	48,945,537
nsv499086	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000007.12	Chr7	48,876,598	48,916,083

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv585560	inversion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv585560	Remapped	Perfect	NC_000007.14:g.488 66456_48905941inv	GRCh38.p12	First Pass	NC_000007.14	Chr7	48,866,456	48,905,941
nssv585560	Remapped	Perfect	NC_000007.13:g.489 06052_48945537inv	GRCh37.p13	First Pass	NC_000007.13	Chr7	48,906,052	48,945,537
nssv585560	Submitted genomic		NC_000007.12:g.488 76598_48916083inv	NCBI36 (hg18)		NC_000007.12	Chr7	48,876,598	48,916,083

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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