A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899762



Internal ID16193718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42886210..43334601hg38UCSC Ensembl
Innerchr19:43390362..43838753hg19UCSC Ensembl
Innerchr19:48082202..48530593hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38448392
hg19448392
hg18448392
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579728
Supporting Variants
Samples
Known GenesLOC284344, PSG11, PSG2, PSG4, PSG5, PSG6, PSG7, PSG9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899762
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