A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061189



Internal ID19150408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59878803..59920042hg38UCSC Ensembl
Innerchr20:58453858..58495097hg19UCSC Ensembl
Innerchr20:57887253..57928492hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3841240
hg1941240
hg1841240
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4337n100
Supporting Variantsnssv3584290, nssv3584287, nssv3584286, nssv3584285, nssv3584291, nssv3584288, nssv3584289
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)nsv1061189
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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