A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1107417



Internal ID15613917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18994964..18999930hg38UCSC Ensembl
Innerchr8:18852474..18857440hg19UCSC Ensembl
Innerchr8:18896754..18901720hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg384967
hg194967
hg184967
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610723
Supporting Variants
Samples
Known GenesPSD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1107417
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