A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604181



Internal ID16391590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:94552455..94777433hg38UCSC Ensembl
Innerchr6:95262173..95487151hg19UCSC Ensembl
Innerchr6:95318894..95543872hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38224979
hg19224979
hg18224979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10845n54
Supporting Variantsnssv1069134
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604181
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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