A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13693388



Internal ID21215239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116633653..116633653hg38UCSC Ensembl
chr10:118393164..118393164hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2788463
Supporting Variants
Samples
Known GenesPNLIPRP2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13693388
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.546875


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