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dbVar

Database of genomic structural variation

nsv6080675

Organism: Homo sapiens

Study:nstd212 (Wu et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Wu et al. 2021

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: 110 SVs from 19 studies. See in: genome view

Submitted genomic111,909,980-111,909,980

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6080675	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	111,909,980	111,909,980
nsv6080675	Remapped	Perfect	GRCh37.p13	Primary Assembly	Second Pass	NC_000011.9	Chr11	111,780,704	111,780,704
nsv6080675	Remapped	Perfect	GRCh37.p13	PATCHES	First Pass	NW_003871080.1	Chr11\|NW_0 03871080.1	161,971	161,971

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17608742	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17608742	Submitted genomic		NC_000011.10:g.111 909980_111909981in s71	GRCh38 (hg38)		NC_000011.10	Chr11	111,909,980	111,909,980
nssv17608742	Remapped	Perfect	NW_003871080.1:g.1 61971_161972ins71	GRCh37.p13	First Pass	NW_003871080.1	Chr11\|NW_0 03871080.1	161,971	161,971
nssv17608742	Remapped	Perfect	NC_000011.9:g.1117 80704_111780705ins 71	GRCh37.p13	Second Pass	NC_000011.9	Chr11	111,780,704	111,780,704

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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