A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604823



Internal ID16392232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:144863368..144893816hg38UCSC Ensembl
Innerchr6:145184504..145214952hg19UCSC Ensembl
Innerchr6:145226197..145256645hg18UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3830449
hg1930449
hg1830449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155789
Samples1798860371_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604823
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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