A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604274



Internal ID16391683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:100630842..100748204hg38UCSC Ensembl
Innerchr6:101078718..101196080hg19UCSC Ensembl
Innerchr6:101185439..101302801hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38117363
hg19117363
hg18117363
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10865n54
Supporting Variantsnssv1070569
Samples
Known GenesASCC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604274
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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