A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv934422



Internal ID16228378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:240923534..240928657hg38UCSC Ensembl
Innerchr2:241862951..241868074hg19UCSC Ensembl
Innerchr2:241511624..241516747hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg385124
hg195124
hg185124
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584900
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv934422
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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