A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13706659



Internal ID21228455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132151337..132151337hg38UCSC Ensembl
chr7:131836096..131836096hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2815894
Supporting Variants
Samples
Known GenesPLXNA4
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13706659
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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