A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603636



Internal ID16044359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:69915274..69984270hg38UCSC Ensembl
Innerchr6:70625166..70694162hg19UCSC Ensembl
Innerchr6:70681887..70750883hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3868997
hg1968997
hg1868997
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154808
Samples1780862194_A
Known GenesCOL19A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603636
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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