A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597606



Internal ID16385015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:24047731..24261846hg38UCSC Ensembl
Innerchr5:24047840..24261955hg19UCSC Ensembl
Innerchr5:24083597..24297712hg18UCSC Ensembl
Cytoband5p14.2
Allele length
AssemblyAllele length
hg38214116
hg19214116
hg18214116
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1027970
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597606
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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