A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603351



Internal ID16390760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:62359158..62463388hg38UCSC Ensembl
Innerchr6:63069063..63173293hg19UCSC Ensembl
Innerchr6:63127022..63231252hg18UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg38104231
hg19104231
hg18104231
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10711n54
Supporting Variantsnssv1154315
SamplesNINDS_125
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603351
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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