A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604268



Internal ID16391677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:100601232..100643558hg38UCSC Ensembl
Innerchr6:101049108..101091434hg19UCSC Ensembl
Innerchr6:101155829..101198155hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3842327
hg1942327
hg1842327
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1070564
Samples
Known GenesASCC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604268
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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