A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564607



Internal ID18516202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:4844193..4945238hg38UCSC Ensembl
Innerchr19:4844205..4945250hg19UCSC Ensembl
Innerchr19:4795205..4896250hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38101046
hg19101046
hg18101046
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065556
Supporting Variants
Samples
Known GenesARRDC5, MIR4747, PLIN3, UHRF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564607
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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