A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584321



Internal ID18882602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59878803..59940597hg38UCSC Ensembl
Innerchr20:58453858..58515652hg19UCSC Ensembl
Innerchr20:57887253..57949047hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3861795
hg1961795
hg1861795
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062669
Supporting Variants
Samples
Known GenesFAM217B, PPP1R3D, SYCP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584321
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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