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dbVar

Database of genomic structural variation

nsv5547210

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:21

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: 141 SVs from 16 studies. See in: genome view

Submitted genomic24,023,990-24,024,010

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5547210	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000018.10	Chr18	24,023,990	24,024,010
nsv5547210	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	21,603,954	21,603,974

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17716669	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17716669	Submitted genomic		NC_000018.10:g.240 23990_24024010ins5 4	GRCh38 (hg38)		NC_000018.10	Chr18	24,023,990	24,024,010
nssv17716669	Remapped	Perfect	NC_000018.9:g.2160 3954_21603974ins54	GRCh37.p13	First Pass	NC_000018.9	Chr18	21,603,954	21,603,974

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)
nssv17716669	<0.001	1	6404

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