A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064770



Internal ID19153989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59878803..59925649hg38UCSC Ensembl
Innerchr20:58453858..58500704hg19UCSC Ensembl
Innerchr20:57887253..57934099hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3846847
hg1946847
hg1846847
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4337n100
Supporting Variantsnssv3584305, nssv3584308, nssv3584307, nssv3584310, nssv3584306, nssv3584309
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)nsv1064770
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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