A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033512



Internal ID19122733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675630..136837737hg38UCSC Ensembl
Innerchr8:137687873..137849980hg19UCSC Ensembl
Innerchr8:137757055..137919162hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38162108
hg19162108
hg18162108
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7325n100
Supporting Variantsnssv3689999, nssv3757483
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)nsv1033512
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