A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586281



Internal ID16027004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54148810..54154632hg38UCSC Ensembl
Innerchr20:52765349..52771171hg19UCSC Ensembl
Innerchr20:52198756..52204578hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg385823
hg195823
hg185823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv941572
Samples
Known GenesCYP24A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586281
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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