A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596803



Internal ID16037526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:1023472..1025735hg38UCSC Ensembl
Innerchr5:1023587..1025850hg19UCSC Ensembl
Innerchr5:1076587..1078850hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg382264
hg192264
hg182264
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1021493
Samples
Known GenesNKD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596803
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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