A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578932



Internal ID16019655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20651291..20807067hg38UCSC Ensembl
Innerchr19:20834097..20989873hg19UCSC Ensembl
Innerchr19:20625937..20781713hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38155777
hg19155777
hg18155777
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6319n54
Supporting Variantsnssv896560, nssv896557, nssv896556, nssv896559, nssv896558
Samples
Known GenesZNF626
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578932
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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