A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579436



Internal ID16020159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36353429..36354362hg38UCSC Ensembl
Innerchr19:36844331..36845264hg19UCSC Ensembl
Innerchr19:41536171..41537104hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38934
hg19934
hg18934
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6427n54
Supporting Variantsnssv899097
Samples
Known GenesZFP14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579436
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