A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3711838



Internal ID19010119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:66691891..66770368hg38UCSC Ensembl
Innerchr13:67266023..67344500hg19UCSC Ensembl
Innerchr13:66164024..66242501hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3878478
hg1978478
hg1878478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050904
Supporting Variants
Samples
Known GenesPCDH9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3711838
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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