A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899122



Internal ID15846392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36354437..36356091hg38UCSC Ensembl
Innerchr19:36845339..36846993hg19UCSC Ensembl
Innerchr19:41537179..41538833hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381655
hg191655
hg181655
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579451
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)nssv899122
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