A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059185



Internal ID19148404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59878803..59931684hg38UCSC Ensembl
Innerchr20:58453858..58506739hg19UCSC Ensembl
Innerchr20:57887253..57940134hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3852882
hg1952882
hg1852882
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4337n100
Supporting Variantsnssv3584319, nssv3584320
Samples
Known GenesSYCP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059185
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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