Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv6289769

Organism: Homo sapiens

Study:nstd214 (Naslavsky 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):Naslavsky 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: 366 SVs from 24 studies. See in: genome view

Submitted genomic77,045,405-77,045,405

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6289769	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000018.10	Chr18	77,045,405	77,045,405
nsv6289769	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	74,757,361	74,757,361

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17942107	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17942107	Submitted genomic		NC_000018.10:g.770 45405_77045406ins8 6	GRCh38 (hg38)		NC_000018.10	Chr18	77,045,405	77,045,405
nssv17942107	Remapped	Perfect	NC_000018.9:g.7475 7361_74757362ins86	GRCh37.p13	First Pass	NC_000018.9	Chr18	74,757,361	74,757,361

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)
nssv17942107	0.016	2	122

You are here: NCBI