A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13689924



Internal ID21211779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76124325..76124325hg38UCSC Ensembl
chr17:74120406..74120406hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2798253
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13689924
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.046875


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