A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1111285



Internal ID15964471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:40327353..40340695hg38UCSC Ensembl
Innerchr8:40184872..40198214hg19UCSC Ensembl
Innerchr8:40304029..40317371hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3813343
hg1913343
hg1813343
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611103
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1111285
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