A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523462



Internal ID18475057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:51747428..52069788hg38UCSC Ensembl
Innerchr13:52321564..52643924hg19UCSC Ensembl
Innerchr13:51219565..51541925hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38322361
hg19322361
hg18322361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044310
Supporting Variants
Samples
Known GenesALG11, ATP7B, CCDC70, DHRS12, LINC00282, NEK5, UTP14C, WDFY2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3523462
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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