A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13677941



Internal ID21199797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50304343..50304343hg38UCSC Ensembl
chr17:48381704..48381704hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2797807
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13677941
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0483871


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