A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066059



Internal ID18808590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:57698779..58288980hg38UCSC Ensembl
Innerchr19:58210147..58800346hg19UCSC Ensembl
Innerchr19:62901959..63492158hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38590202
hg19590200
hg18590200
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3570456
Samples
Known GenesC19orf18, FKBP1AP1, LOC100128398, ZNF135, ZNF154, ZNF256, ZNF274, ZNF329, ZNF417, ZNF418, ZNF544, ZNF552, ZNF586, ZNF587, ZNF587B, ZNF606, ZNF671, ZNF776, ZNF8, ZNF814, ZSCAN1, ZSCAN18
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066059
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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