A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603435



Internal ID16390844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65342401..65381458hg38UCSC Ensembl
Innerchr6:66052294..66091351hg19UCSC Ensembl
Innerchr6:66109015..66148072hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3839058
hg1939058
hg1839058
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10725n54
Supporting Variantsnssv1062632
Samples
Known GenesEYS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603435
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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