A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067289



Internal ID19156508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59878803..59919660hg38UCSC Ensembl
Innerchr20:58453858..58494715hg19UCSC Ensembl
Innerchr20:57887253..57928110hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3840858
hg1940858
hg1840858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4337n100
Supporting Variantsnssv3584284
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)nsv1067289
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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