A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058882



Internal ID18801413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54149440..54177833hg38UCSC Ensembl
Innerchr20:52765979..52794372hg19UCSC Ensembl
Innerchr20:52199386..52227779hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3828394
hg1928394
hg1828394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3587569, nssv3587568
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)nsv1058882
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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