A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2915568



Internal ID15734622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:111573116..111574724hg38UCSC Ensembl
Innerchr5:110908813..110910421hg19UCSC Ensembl
Innerchr5:110936712..110938320hg18UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg381609
hg191609
hg181609
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514318
Supporting Variants
SamplesNA19118
Known GenesSTARD4-AS1
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2915568
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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