A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3587568



Internal ID18539163
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 StatusS
Merged Variantsnsv1058882
Supporting Variants
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)nssv3587568
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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