A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13681191



Internal ID21203051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:97132609..97132609hg38UCSC Ensembl
chr12:97526387..97526387hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2791769
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13681191
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.03125


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