A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603436



Internal ID16390845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65342401..65405761hg38UCSC Ensembl
Innerchr6:66052294..66115654hg19UCSC Ensembl
Innerchr6:66109015..66172375hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3863361
hg1963361
hg1863361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10726n54
Supporting Variantsnssv1062633
Samples
Known GenesEYS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603436
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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