A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603695



Internal ID16044418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:73702325..74066188hg38UCSC Ensembl
Innerchr6:74412048..74775904hg19UCSC Ensembl
Innerchr6:74468769..74832624hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38363864
hg19363857
hg18363856
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154321
Samples1780862347_A
Known GenesCD109
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603695
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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