A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899862



Internal ID16193818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43158934..43335936hg38UCSC Ensembl
Innerchr19:43663086..43840088hg19UCSC Ensembl
Innerchr19:48354926..48531928hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38177003
hg19177003
hg18177003
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579816
Supporting Variants
Samples
Known GenesLOC284344, PSG4, PSG5, PSG9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899862
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