A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020673



Internal ID19109892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:51966386..52004909hg38UCSC Ensembl
Innerchr8:52878946..52917469hg19UCSC Ensembl
Innerchr8:53041499..53080022hg18UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3838524
hg1938524
hg1838524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7217n100
Supporting Variantsnssv3687497, nssv3687496
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)nsv1020673
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer