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dbVar

Database of genomic structural variation

nsv94675

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:9,500

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: 175 SVs from 47 studies. See in: genome view

Remapped(Score: Perfect):58,872,682-58,882,181

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv94675	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000015.10	Chr15	58,872,682	58,882,181
nsv94675	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	59,164,881	59,174,380
nsv94675	Submitted genomic		NCBI35 (hg17)	Primary Assembly		NC_000015.8	Chr15	56,952,173	56,961,672

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv113253	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv113253	Remapped	Perfect	NC_000015.10:g.588 72682_58882181del9 500	GRCh38.p12	First Pass	NC_000015.10	Chr15	58,872,682	58,882,181
nssv113253	Remapped	Perfect	NC_000015.9:g.5916 4881_59174380del95 00	GRCh37.p13	First Pass	NC_000015.9	Chr15	59,164,881	59,174,380
nssv113253	Submitted genomic		NC_000015.8:g.5695 2173_56961672del95 00	NCBI35 (hg17)		NC_000015.8	Chr15	56,952,173	56,961,672

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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