A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057861



Internal ID19147080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:57759836..57871008hg38UCSC Ensembl
Innerchr19:58271204..58382376hg19UCSC Ensembl
Innerchr19:62963016..63074188hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38111173
hg19111173
hg18111173
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3686n100
Supporting Variantsnssv3570457
Samples
Known GenesFKBP1AP1, ZNF552, ZNF586, ZNF587, ZNF587B, ZNF814
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057861
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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