A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv933821



Internal ID16227777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:240031005..240041845hg38UCSC Ensembl
Innerchr2:240970422..240981262hg19UCSC Ensembl
Innerchr2:240619095..240629935hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3810841
hg1910841
hg1810841
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584801
Supporting Variants
Samples
Known GenesPRR21
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv933821
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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