A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13682907



Internal ID21204764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78111932..78111932hg38UCSC Ensembl
chr17:76108013..76108013hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2797210
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13682907
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.178571


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