A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578930



Internal ID16019653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20651291..20799821hg38UCSC Ensembl
Innerchr19:20834097..20982627hg19UCSC Ensembl
Innerchr19:20625937..20774467hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38148531
hg19148531
hg18148531
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6319n54
Supporting Variantsnssv896549
Samples
Known GenesZNF626
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578930
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer