A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604266



Internal ID16391675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:100588837..100711074hg38UCSC Ensembl
Innerchr6:101036713..101158950hg19UCSC Ensembl
Innerchr6:101143434..101265671hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38122238
hg19122238
hg18122238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10864n54
Supporting Variantsnssv1070563
Samples
Known GenesASCC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604266
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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