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dbVar

Database of genomic structural variation

nsv481402

Organism: Homo sapiens

Study:nstd35 (Kidd et al. 2010)
Variant Type:novel sequence insertion
Method Type:Sequencing
Variant is Defined by:GU268907

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:839

Description:This variant by definition has no placement. It represents a contig assembled from multiple read pairs, no part of which could be mapped to assembly NCBI35.
Publication(s):Kidd et al. 2010

Links to Other Resources

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Remapped(Score: Good):35,116,791-35,117,629

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Sequence ID	Chr	Start	Stop
nsv481402	Remapped	Good	GRCh38.p12	Primary Assembly	NT_025741.16	Chr6\|NT_02 5741.16	35,116,791	35,117,629

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv3019003	novel sequence insertion	Sequencing	One end anchored assembly

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Sequence ID	Chr	Start	Stop
nssv3019003	Remapped	Good	NT_025741.16:g.351 16791_35117629ins?	GRCh38.p12	NT_025741.16	Chr6\|NT_02 5741.16	35,116,791	35,117,629

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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