A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv901099



Internal ID15848369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:52871534..52898507hg38UCSC Ensembl
Innerchr19:53374787..53401760hg19UCSC Ensembl
Innerchr19:58066599..58093572hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3826974
hg1926974
hg1826974
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580045
Supporting Variants
Samples
Known GenesZNF320
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv901099
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