A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584253



Internal ID18535848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59844304..59931684hg38UCSC Ensembl
Innerchr20:58419359..58506739hg19UCSC Ensembl
Innerchr20:57852754..57940134hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3887381
hg1987381
hg1887381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058271
Supporting Variants
Samples
Known GenesPHACTR3, SYCP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584253
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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