A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13702701



Internal ID21224521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:61505654..61505654hg38UCSC Ensembl
chr5:60801481..60801481hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2811811
Supporting Variants
Samples
Known GenesZSWIM6
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13702701
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0434783


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