A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv930959



Internal ID16224915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:212272022..212346343hg38UCSC Ensembl
Innerchr2:213136747..213211067hg19UCSC Ensembl
Innerchr2:212844992..212919312hg18UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3874322
hg1974321
hg1874321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584355
Supporting Variants
Samples
Known GenesERBB4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv930959
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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