A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601005



Internal ID16388414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:14840332..14845568hg38UCSC Ensembl
Innerchr6:14840563..14845799hg19UCSC Ensembl
Innerchr6:14948542..14953778hg18UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg385237
hg195237
hg185237
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1049444, nssv1049445
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601005
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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