A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13702254



Internal ID21224077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:102044515..102044515hg38UCSC Ensembl
chr3:101763359..101763359hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38985
hg19985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2806735
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13702254
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.71875


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