A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057519



Internal ID18800050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:37386619..37449058hg38UCSC Ensembl
Innerchr20:36015022..36077460hg19UCSC Ensembl
Innerchr20:35448436..35510874hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3862440
hg1962439
hg1862439
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4306n100
Supporting Variantsnssv3584760
Samples
Known GenesSRC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057519
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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