A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597428



Internal ID16384837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:20058820..20114497hg38UCSC Ensembl
Innerchr5:20058929..20114606hg19UCSC Ensembl
Innerchr5:20094686..20150363hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3855678
hg1955678
hg1855678
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1026835
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597428
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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