A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061252



Internal ID19150471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:483143..524933hg38UCSC Ensembl
Innerchr20:463787..505577hg19UCSC Ensembl
Innerchr20:411787..453577hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3841791
hg1941791
hg1841791
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4222n100
Supporting Variantsnssv3589958
Samples
Known GenesCSNK2A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061252
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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