A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062636



Internal ID19151855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59878803..59928674hg38UCSC Ensembl
Innerchr20:58453858..58503729hg19UCSC Ensembl
Innerchr20:57887253..57937124hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3849872
hg1949872
hg1849872
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4337n100
Supporting Variantsnssv3584316, nssv3584315, nssv3584318, nssv3584314, nssv3584317
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)nsv1062636
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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