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dbVar

Database of genomic structural variation

nsv5535010

Organism: Homo sapiens

Study:nstd206 (Byrska-Bishop et al. 2022)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Byrska-Bishop et al. 2022

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: 147 SVs from 29 studies. See in: genome view

Submitted genomic70,461,090-70,461,090

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5535010	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	70,461,090	70,461,090
nsv5535010	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	70,494,993	70,494,993

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17707209	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17707209	Submitted genomic		NC_000016.10:g.704 61090_70461091ins3 42	GRCh38 (hg38)		NC_000016.10	Chr16	70,461,090	70,461,090
nssv17707209	Remapped	Perfect	NC_000016.9:g.7049 4993_70494994ins34 2	GRCh37.p13	First Pass	NC_000016.9	Chr16	70,494,993	70,494,993

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv17707209	<0.001	1	6404

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