A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv930955



Internal ID16224911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:212253251..212327936hg38UCSC Ensembl
Innerchr2:213117976..213192660hg19UCSC Ensembl
Innerchr2:212826221..212900905hg18UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3874686
hg1974685
hg1874685
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584348
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)nssv930955
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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