A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597715



Internal ID16385124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:28779250..28868356hg38UCSC Ensembl
Innerchr5:28779357..28868463hg19UCSC Ensembl
Innerchr5:28815114..28904220hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3889107
hg1989107
hg1889107
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9706n54
Supporting Variantsnssv1028708
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597715
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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