A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597738



Internal ID16385147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:28811682..28902719hg38UCSC Ensembl
Innerchr5:28811789..28902826hg19UCSC Ensembl
Innerchr5:28847546..28938583hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3891038
hg1991038
hg1891038
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9709n54
Supporting Variantsnssv1153309
SamplesNINDS_142
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597738
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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