A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1023660



Internal ID16317616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:2279564..2337225hg38UCSC Ensembl
Innerchr5:2279678..2337339hg19UCSC Ensembl
Innerchr5:2332678..2390339hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3857662
hg1957662
hg1857662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596909
Supporting Variants
Samples
Known GenesLOC100506858
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1023660
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