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dbVar

Database of genomic structural variation

nsv39544

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:9,818

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: 310 SVs from 63 studies. See in: genome view

Remapped(Score: Perfect):48,425,555-48,435,372

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv39544	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	48,425,555	48,435,372
nsv39544	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	48,447,107	48,456,924
nsv39544	Submitted genomic		NCBI35 (hg17)	Primary Assembly		NC_000011.8	Chr11	48,403,683	48,413,500

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv58122	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv58122	Remapped	Perfect	NC_000011.10:g.484 25555_48435372del9 818	GRCh38.p12	First Pass	NC_000011.10	Chr11	48,425,555	48,435,372
nssv58122	Remapped	Perfect	NC_000011.9:g.4844 7107_48456924del98 18	GRCh37.p13	First Pass	NC_000011.9	Chr11	48,447,107	48,456,924
nssv58122	Submitted genomic		NC_000011.8:g.4840 3683_48413500del98 18	NCBI35 (hg17)		NC_000011.8	Chr11	48,403,683	48,413,500

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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