A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059126



Internal ID19148345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:8731363..8819463hg38UCSC Ensembl
Innerchr19:8841725..8930139hg19UCSC Ensembl
Innerchr19:8702725..8791139hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3888101
hg1988415
hg1888415
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564681
Samples
Known GenesOR2Z1, ZNF558
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059126
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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