A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899111



Internal ID15846381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36354437..36355281hg38UCSC Ensembl
Innerchr19:36845339..36846183hg19UCSC Ensembl
Innerchr19:41537179..41538023hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38845
hg19845
hg18845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579447
Supporting Variants
Samples
Known GenesZFP14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899111
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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