A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032266



Internal ID19121488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:87278365..87429746hg38UCSC Ensembl
Innerchr8:88290593..88441974hg19UCSC Ensembl
Innerchr8:88359709..88511090hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38151382
hg19151382
hg18151382
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757318
Samples
Known GenesCNBD1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032266
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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