A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597878



Internal ID16385287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:41229175..41234541hg38UCSC Ensembl
Innerchr5:41229277..41234643hg19UCSC Ensembl
Innerchr5:41265034..41270400hg18UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg385367
hg195367
hg185367
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153344
SamplesHGDP01223
Known GenesC6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597878
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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