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dbVar

Database of genomic structural variation

nsv84479

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:9,594

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: 90 SVs from 28 studies. See in: genome view

Remapped(Score: Perfect):49,056,071-49,065,664

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv84479	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000014.9	Chr14	49,056,071	49,065,664
nsv84479	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	49,522,789	49,532,382
nsv84479	Submitted genomic		NCBI35 (hg17)	Primary Assembly		NC_000014.7	Chr14	48,592,539	48,602,132

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv103057	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv103057	Remapped	Perfect	NC_000014.9:g.4905 6071_49065664del95 94	GRCh38.p12	First Pass	NC_000014.9	Chr14	49,056,071	49,065,664
nssv103057	Remapped	Perfect	NC_000014.8:g.4952 2789_49532382del95 94	GRCh37.p13	First Pass	NC_000014.8	Chr14	49,522,789	49,532,382
nssv103057	Submitted genomic		NC_000014.7:g.4859 2539_48602132del95 94	NCBI35 (hg17)		NC_000014.7	Chr14	48,592,539	48,602,132

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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