A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584323



Internal ID16371732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:211866789..211918450hg38UCSC Ensembl
Innerchr2:212731514..212783175hg19UCSC Ensembl
Innerchr2:212439759..212491420hg18UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3851662
hg1951662
hg1851662
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv930910
Samples
Known GenesERBB4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584323
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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