A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604093



Internal ID16044816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:85495605..85570019hg38UCSC Ensembl
Innerchr6:86205323..86279737hg19UCSC Ensembl
Innerchr6:86262042..86336456hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3874415
hg1974415
hg1874415
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154843
SamplesHGDP00208
Known GenesNT5E, SNX14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604093
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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