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dbVar

Database of genomic structural variation

nsv81421

Organism: Homo sapiens

Study:nstd6 (Mills et al. 2006)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:NCBI35 (hg17)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:2

Publication(s):Mills et al. 2006

Links to Other Resources

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: 113 SVs from 29 studies. See in: genome view

Remapped(Score: Perfect):32,483,421-32,483,422

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv81421	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000014.9	Chr14	32,483,421	32,483,422
nsv81421	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	32,952,627	32,952,628
nsv81421	Submitted genomic		NCBI35 (hg17)	Primary Assembly		NC_000014.7	Chr14	32,022,378	32,022,379

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv99999	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv99999	Remapped	Perfect	NC_000014.9:g.3248 3421_32483422delAC	GRCh38.p12	First Pass	NC_000014.9	Chr14	32,483,421	32,483,422
nssv99999	Remapped	Perfect	NC_000014.8:g.3295 2627_32952628delAC	GRCh37.p13	First Pass	NC_000014.8	Chr14	32,952,627	32,952,628
nssv99999	Submitted genomic		NC_000014.7:g.3202 2378_32022379delAC	NCBI35 (hg17)		NC_000014.7	Chr14	32,022,378	32,022,379

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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