A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063056



Internal ID19152275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59878803..59924532hg38UCSC Ensembl
Innerchr20:58453858..58499587hg19UCSC Ensembl
Innerchr20:57887253..57932982hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3845730
hg1945730
hg1845730
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4337n100
Supporting Variantsnssv3584298
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)nsv1063056
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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