A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060714



Internal ID19149933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59851494..59920042hg38UCSC Ensembl
Innerchr20:58426549..58495097hg19UCSC Ensembl
Innerchr20:57859944..57928492hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3868549
hg1968549
hg1868549
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4335n100
Supporting Variantsnssv3584268, nssv3584269
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)nsv1060714
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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