A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13711245



Internal ID21233006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77586987..77586987hg38UCSC Ensembl
chr5:76882812..76882812hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38376
hg19376
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2811854
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13711245
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.78125


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