A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13680325



Internal ID21202188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8912173..8912173hg38UCSC Ensembl
chr1:8972232..8972232hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2801712
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13680325
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.296875


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