A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579443



Internal ID16020166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36354362..36355098hg38UCSC Ensembl
Innerchr19:36845264..36846000hg19UCSC Ensembl
Innerchr19:41537104..41537840hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38737
hg19737
hg18737
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6429n54
Supporting Variantsnssv899105, nssv899106
Samples
Known GenesZFP14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579443
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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