A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020914



Internal ID19110132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:93269582..93303098hg38UCSC Ensembl
Innerchr8:94281810..94315326hg19UCSC Ensembl
Innerchr8:94350986..94384502hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3833517
hg1933517
hg1833517
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7269n100
Supporting Variantsnssv3689721
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)nsv1020914
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