A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3571743



Internal ID18870024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43015210..43226065hg38UCSC Ensembl
Innerchr19:43519362..43730217hg19UCSC Ensembl
Innerchr19:48211202..48422057hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38210856
hg19210856
hg18210856
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065672
Supporting Variants
Samples
Known GenesLOC284344, PSG11, PSG2, PSG4, PSG5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3571743
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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