A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059035



Internal ID19148254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59847994..59924573hg38UCSC Ensembl
Innerchr20:58423049..58499628hg19UCSC Ensembl
Innerchr20:57856444..57933023hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3876580
hg1976580
hg1876580
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4335n100
Supporting Variantsnssv3584262
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)nsv1059035
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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