A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596979



Internal ID16384388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:7169738..7193343hg38UCSC Ensembl
Innerchr5:7169851..7193456hg19UCSC Ensembl
Innerchr5:7222851..7246456hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3823606
hg1923606
hg1823606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9560n54
Supporting Variantsnssv1023782
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596979
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