A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604269



Internal ID16391678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:100611010..100675627hg38UCSC Ensembl
Innerchr6:101058886..101123503hg19UCSC Ensembl
Innerchr6:101165607..101230224hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3864618
hg1964618
hg1864618
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155781
Samples1782681096_A
Known GenesASCC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604269
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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