A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580403



Internal ID16021126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:58058263..58108701hg38UCSC Ensembl
Innerchr19:58569631..58620068hg19UCSC Ensembl
Innerchr19:63261443..63311880hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3850439
hg1950438
hg1850438
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv901995
Samples
Known GenesZNF135, ZSCAN18
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580403
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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