A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055845



Internal ID19145064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:57806061..57865008hg38UCSC Ensembl
Innerchr19:58317429..58376376hg19UCSC Ensembl
Innerchr19:63009241..63068188hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3858948
hg1958948
hg1858948
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3570458
Samples
Known GenesFKBP1AP1, ZNF552, ZNF587, ZNF587B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055845
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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