A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv933667



Internal ID15880937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:237542799..237545129hg38UCSC Ensembl
Innerchr2:238451442..238453772hg19UCSC Ensembl
Innerchr2:238116181..238118511hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg382331
hg192331
hg182331
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584736
Supporting Variants
Samples
Known GenesMLPH
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv933667
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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