A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596980



Internal ID16384389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:7169738..7200104hg38UCSC Ensembl
Innerchr5:7169851..7200217hg19UCSC Ensembl
Innerchr5:7222851..7253217hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3830367
hg1930367
hg1830367
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9560n54
Supporting Variantsnssv1023783
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596980
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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