A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1652n100



Internal ID20153268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51747428..52069788hg38UCSC Ensembl
chr13:52321564..52643924hg19UCSC Ensembl
chr13:51219565..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 StatusM
Merged Variants
Supporting Variantsnsv1044310, nsv1050117
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)dgv1652n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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