A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17522258



Internal ID21846617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:238397745..238397745hg38UCSC Ensembl
chr2:239306386..239306386hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38240
hg19240
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6057053
Supporting Variants
Samples
Known GenesTRAF3IP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17522258
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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