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dbVar

Database of genomic structural variation

nsv513729

Organism: Homo sapiens

Study:nstd50 (Arlt et al. 2011)
Variant Type:insertion
Method Type:Sequencing
Submitted on:NCBI36 (hg18)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:2,806

Publication(s):Arlt et al. 2011

Links to Other Resources

Overlapping Genes

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: 277 SVs from 60 studies. See in: genome view

Remapped(Score: Perfect):788,752-791,557

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nsv513729	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	788,752	791,557
nsv513729	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	724,132	726,937
nsv513729	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000001.9	Chr1	713,995	716,800

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv626981	insertion	1	Sequencing	Paired-end mapping	2,637

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nssv626981	Remapped	Perfect	NC_000001.11:g.(78 8752_?)_(?_791557) ins2806	GRCh38.p12	First Pass	NC_000001.11	Chr1	788,752	791,557
nssv626981	Remapped	Perfect	NC_000001.10:g.(72 4132_?)_(?_726937) ins2806	GRCh37.p13	First Pass	NC_000001.10	Chr1	724,132	726,937
nssv626981	Submitted genomic		NC_000001.9:g.(713 995_?)_(?_716800)i ns2806	NCBI36 (hg18)		NC_000001.9	Chr1	713,995	716,800

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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