A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015350



Internal ID19104567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:818461..914408hg38UCSC Ensembl
Innerchr8:768461..864408hg19UCSC Ensembl
Innerchr8:758461..854408hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3895948
hg1995948
hg1895948
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3675030
Samples
Known GenesERICH1-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015350
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