A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580402



Internal ID16021125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:57622904..57704099hg38UCSC Ensembl
Innerchr19:58134272..58215467hg19UCSC Ensembl
Innerchr19:62826084..62907279hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3881196
hg1981196
hg1881196
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv901994
Samples
Known GenesZNF154, ZNF211, ZNF551, ZSCAN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580402
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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