A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv941814



Internal ID16235770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59888938..59923262hg38UCSC Ensembl
Innerchr20:58463993..58498317hg19UCSC Ensembl
Innerchr20:57897388..57931712hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3834325
hg1934325
hg1834325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586371
Supporting Variants
Samples
Known GenesSYCP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv941814
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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