A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598827



Internal ID16386236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:85177970..85220596hg38UCSC Ensembl
Innerchr5:84473788..84516414hg19UCSC Ensembl
Innerchr5:84509544..84552170hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3842627
hg1942627
hg1842627
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153961
SamplesHGDP00963
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598827
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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