A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605529



Internal ID16392938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:169806629..169854950hg38UCSC Ensembl
Innerchr6:170206725..170255046hg19UCSC Ensembl
Innerchr6:169948650..169996971hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3848322
hg1948322
hg1848322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155823
SamplesNINDS_74
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605529
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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