A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604792



Internal ID16045515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:141871588..142078114hg38UCSC Ensembl
Innerchr6:142192725..142399251hg19UCSC Ensembl
Innerchr6:142234418..142440944hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38206527
hg19206527
hg18206527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1074135
Samples
Known GenesNMBR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604792
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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