A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3526804



Internal ID18825085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:64807508..64911423hg38UCSC Ensembl
Innerchr13:65381640..65485555hg19UCSC Ensembl
Innerchr13:64279641..64383556hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38103916
hg19103916
hg18103916
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037234
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3526804
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