A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13692721



Internal ID21214571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:167214091..167214197hg38UCSC Ensembl
chr2:168070601..168070707hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2805639
Supporting Variants
Samples
Known GenesXIRP2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13692721
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.196429


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