A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063981



Internal ID18806512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54148778..54160074hg38UCSC Ensembl
Innerchr20:52765317..52776613hg19UCSC Ensembl
Innerchr20:52198724..52210020hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3811297
hg1911297
hg1811297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3731492
Samples
Known GenesCYP24A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063981
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