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dbVar

Database of genomic structural variation

nsv499765

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:16,719

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: 214 SVs from 42 studies. See in: genome view

Remapped(Score: Perfect):233,562,199-233,578,917

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv499765	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000002.12	Chr2	233,562,199	233,578,917
nsv499765	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	234,470,297	234,487,015
nsv499765	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000002.10	Chr2	234,135,584	234,152,302

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv585536	inversion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv585536	Remapped	Perfect	NC_000002.12:g.233 562199_233578917in v	GRCh38.p12	First Pass	NC_000002.12	Chr2	233,562,199	233,578,917
nssv585536	Remapped	Perfect	NC_000002.11:g.234 470297_234487015in v	GRCh37.p13	First Pass	NC_000002.11	Chr2	234,470,297	234,487,015
nssv585536	Submitted genomic		NC_000002.10:g.234 135584_234152302in v	NCBI36 (hg18)		NC_000002.10	Chr2	234,135,584	234,152,302

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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