A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059559



Internal ID18802090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59862589..59922116hg38UCSC Ensembl
Innerchr20:58437644..58497171hg19UCSC Ensembl
Innerchr20:57871039..57930566hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3859528
hg1959528
hg1859528
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4336n100
Supporting Variantsnssv3584280, nssv3584278, nssv3584279
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)nsv1059559
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer