A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584355



Internal ID16371764
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 StatusM
Merged Variantsdgv7275n54
Supporting Variantsnssv930959
Samples
Known GenesERBB4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584355
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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