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dbVar

Database of genomic structural variation

nsv159446

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:9,784

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: 151 SVs from 35 studies. See in: genome view

Remapped(Score: Perfect):15,174,383-15,184,166

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv159446	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	15,174,383	15,184,166
nsv159446	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	15,500,879	15,510,662
nsv159446	Submitted genomic		NCBI35 (hg17)	Primary Assembly		NC_000001.8	Chr1	15,246,185	15,255,968

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv178024	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv178024	Remapped	Perfect	NC_000001.11:g.151 74383_15184166del9 784	GRCh38.p12	First Pass	NC_000001.11	Chr1	15,174,383	15,184,166
nssv178024	Remapped	Perfect	NC_000001.10:g.155 00879_15510662del9 784	GRCh37.p13	First Pass	NC_000001.10	Chr1	15,500,879	15,510,662
nssv178024	Submitted genomic		NC_000001.8:g.1524 6185_15255968del97 84	NCBI35 (hg17)		NC_000001.8	Chr1	15,246,185	15,255,968

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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