A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030947



Internal ID19120167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:53622673..53679513hg38UCSC Ensembl
Innerchr8:54535233..54592073hg19UCSC Ensembl
Innerchr8:54697786..54754626hg18UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3856841
hg1956841
hg1856841
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7226n100
Supporting Variantsnssv3757268
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030947
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