A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596713



Internal ID16384122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:668222..696435hg38UCSC Ensembl
Innerchr5:668337..696550hg19UCSC Ensembl
Innerchr5:721337..749550hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3828214
hg1928214
hg1828214
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9497n54
Supporting Variantsnssv1021335
Samples
Known GenesTPPP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596713
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer