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dbVar

Database of genomic structural variation

nsv6082136

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: 125 SVs from 17 studies. See in: genome view

Submitted genomic41,901,501-41,901,501

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6082136	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	41,901,501	41,901,501
nsv6082136	Remapped	Perfect	GRCh37.p13	Primary Assembly	Second Pass	NC_000017.10	Chr17	40,057,754	40,057,754
nsv6082136	Remapped	Perfect	GRCh37.p13	PATCHES	First Pass	NW_003571052.1	Chr17\|NW_0 03571052.1	188,143	188,143

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17623148	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17623148	Submitted genomic		NC_000017.11:g.419 01501_41901502ins2 77	GRCh38 (hg38)		NC_000017.11	Chr17	41,901,501	41,901,501
nssv17623148	Remapped	Perfect	NW_003571052.1:g.1 88143_188144ins277	GRCh37.p13	First Pass	NW_003571052.1	Chr17\|NW_0 03571052.1	188,143	188,143
nssv17623148	Remapped	Perfect	NC_000017.10:g.400 57754_40057755ins2 77	GRCh37.p13	Second Pass	NC_000017.10	Chr17	40,057,754	40,057,754

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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