A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15203682



Internal ID21342486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105908615..105908615hg38UCSC Ensembl
chr7:105549061..105549061hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3953722
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15203682
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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