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dbVar

Database of genomic structural variation

nsv4730242

Organism: Homo sapiens

Study:nstd198 (Hanlon et al. 2021)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:22,408

Publication(s):Hanlon 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: 928 SVs from 69 studies. See in: genome view

Submitted genomic103,711,851-103,734,258

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4730242	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	103,711,851	103,734,258
nsv4730242	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	104,254,473	104,276,880

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
nssv16255918	inversion	HG00512	Sequencing	Genotyping	Heterozygous	328

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16255918	Submitted genomic		NC_000001.11:g.103 711851_103734258in v	GRCh38 (hg38)		NC_000001.11	Chr1	103,711,851	103,734,258
nssv16255918	Remapped	Perfect	NC_000001.10:g.104 254473_104276880in v	GRCh37.p13	First Pass	NC_000001.10	Chr1	104,254,473	104,276,880

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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