A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061029



Internal ID18803560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51746647..52111494hg38UCSC Ensembl
Innerchr19:52249900..52614747hg19UCSC Ensembl
Innerchr19:56941712..57306559hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38364848
hg19364848
hg18364848
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3626n100
Supporting Variantsnssv3724912
Samples
Known GenesFPR1, FPR2, 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)nsv1061029
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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