A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059263



Internal ID18801794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51770004..52104518hg38UCSC Ensembl
Innerchr19:52273257..52607771hg19UCSC Ensembl
Innerchr19:56965069..57299583hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38334515
hg19334515
hg18334515
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3626n100
Supporting Variantsnssv3575020
Samples
Known GenesFPR2, FPR3, HCCAT3, ZNF350, ZNF432, ZNF577, ZNF613, ZNF614, ZNF615, ZNF649, ZNF841
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059263
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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