A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605507



Internal ID16392916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:169633437..169691613hg38UCSC Ensembl
Innerchr6:170033533..170091709hg19UCSC Ensembl
Innerchr6:169775458..169833634hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3858177
hg1958177
hg1858177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155822
Samples1780862444_A
Known GenesWDR27
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605507
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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