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dbVar

Database of genomic structural variation

nsv39282

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:9,869

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: 272 SVs from 64 studies. See in: genome view

Remapped(Score: Perfect):55,823,248-55,833,116

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv39282	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	55,823,248	55,833,116
nsv39282	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	55,590,724	55,600,592
nsv39282	Submitted genomic		NCBI35 (hg17)	Primary Assembly		NC_000011.8	Chr11	55,347,300	55,357,168

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv57860	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv57860	Remapped	Perfect	NC_000011.10:g.558 23248_55833116del9 869	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,823,248	55,833,116
nssv57860	Remapped	Perfect	NC_000011.9:g.5559 0724_55600592del98 69	GRCh37.p13	First Pass	NC_000011.9	Chr11	55,590,724	55,600,592
nssv57860	Submitted genomic		NC_000011.8:g.5534 7300_55357168del98 69	NCBI35 (hg17)		NC_000011.8	Chr11	55,347,300	55,357,168

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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