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dbVar

Database of genomic structural variation

nsv5538763

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: 99 SVs from 23 studies. See in: genome view

Submitted genomic100,026,381-100,026,381

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5538763	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000014.9	Chr14	100,026,381	100,026,381
nsv5538763	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	100,492,718	100,492,718

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17697368	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17697368	Submitted genomic		NC_000014.9:g.1000 26381_100026382ins 186	GRCh38 (hg38)		NC_000014.9	Chr14	100,026,381	100,026,381
nssv17697368	Remapped	Perfect	NC_000014.8:g.1004 92718_100492719ins 186	GRCh37.p13	First Pass	NC_000014.8	Chr14	100,492,718	100,492,718

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)
nssv17697368	0.093	589	6348

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