A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13684940



Internal ID21206800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:238397772..238397772hg38UCSC Ensembl
chr2:239306413..239306413hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2807240
Supporting Variants
Samples
Known GenesTRAF3IP1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13684940
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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