A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604601



Internal ID16392010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:125293275..125316237hg38UCSC Ensembl
Innerchr6:125614421..125637383hg19UCSC Ensembl
Innerchr6:125656120..125679082hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3822963
hg1922963
hg1822963
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1072399
Samples
Known GenesHDDC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604601
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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