A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603472



Internal ID16390881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65781163..65889045hg38UCSC Ensembl
Innerchr6:66491056..66598938hg19UCSC Ensembl
Innerchr6:66547777..66655659hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38107883
hg19107883
hg18107883
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153714
SamplesHGDP00818
Known GenesSLC25A51P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603472
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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