A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15192507



Internal ID21331390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:97156980..97156980hg38UCSC Ensembl
chr12:97550758..97550758hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3953068
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15192507
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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