A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025247



Internal ID19114465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:60086171..60097568hg38UCSC Ensembl
Innerchr8:60998730..61010127hg19UCSC Ensembl
Innerchr8:61161284..61172681hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3811398
hg1911398
hg1811398
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7234n100
Supporting Variantsnssv3689465
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)nsv1025247
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