A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579449



Internal ID16020172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36354437..36355740hg38UCSC Ensembl
Innerchr19:36845339..36846642hg19UCSC Ensembl
Innerchr19:41537179..41538482hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381304
hg191304
hg181304
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6428n54
Supporting Variantsnssv899117, nssv899114, nssv899118, nssv899116, nssv899115
Samples
Known GenesZFP14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579449
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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