A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584312



Internal ID18882593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59878803..59927593hg38UCSC Ensembl
Innerchr20:58453858..58502648hg19UCSC Ensembl
Innerchr20:57887253..57936043hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3848791
hg1948791
hg1848791
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065356
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)nssv3584312
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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