A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584269



Internal ID18882550
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 StatusS
Merged Variantsnsv1060714
Supporting Variants
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)nssv3584269
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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