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dbVar

Database of genomic structural variation

nsv3060307

Organism: Homo sapiens

Study:nstd140 (Fan et al. 2017)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

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

Publication(s):Fan et al. 2017

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: 328 SVs from 27 studies. See in: genome view

Remapped(Score: Perfect):63,264,906-63,264,906

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv3060307	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000018.10	Chr18	63,264,906	63,264,906
nsv3060307	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000018.9	Chr18	60,932,139	60,932,139

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv14022013	insertion	CHM1	Sequencing	Local sequence assembly	7,551

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv14022013	Remapped	Perfect	NC_000018.10:g.632 64906_63264907ins1 05	GRCh38.p12	First Pass	NC_000018.10	Chr18	63,264,906	63,264,906
nssv14022013	Submitted genomic		NC_000018.9:g.6093 2139_60932140ins10 5	GRCh37 (hg19)		NC_000018.9	Chr18	60,932,139	60,932,139

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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