A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604839



Internal ID16045562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:145984674..146507786hg38UCSC Ensembl
Innerchr6:146305810..146828922hg19UCSC Ensembl
Innerchr6:146347503..146870615hg18UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38523113
hg19523113
hg18523113
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1074345
Samples
Known GenesGRM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604839
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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