A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597935



Internal ID16385344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:44876186..44916687hg38UCSC Ensembl
Innerchr5:44876288..44916789hg19UCSC Ensembl
Innerchr5:44912045..44952546hg18UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3840502
hg1940502
hg1840502
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9739n54
Supporting Variantsnssv1153534
Samples1798860072_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597935
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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