A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15191968



Internal ID21330832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:65741580..65741580hg38UCSC Ensembl
chr12:66135360..66135360hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3954169
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15191968
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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