A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025578



Internal ID19114796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:69051049..69073572hg38UCSC Ensembl
Innerchr8:69963284..69985807hg19UCSC Ensembl
Innerchr8:70125838..70148361hg18UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg3822524
hg1922524
hg1822524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689509
Samples
Known GenesLOC100505718
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025578
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