A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15202972



Internal ID21341741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:924160..924160hg38UCSC Ensembl
chr7:963796..963796hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3930177
Supporting Variants
SamplesHG002
Known GenesADAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15202972
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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