A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060589



Internal ID18803120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59851494..59922116hg38UCSC Ensembl
Innerchr20:58426549..58497171hg19UCSC Ensembl
Innerchr20:57859944..57930566hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3870623
hg1970623
hg1870623
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4335n100
Supporting Variantsnssv3584270, nssv3584271
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)nsv1060589
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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