A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527032



Internal ID15107639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:119421736..119437757hg38UCSC Ensembl
Innerchr8:120433976..120449997hg19UCSC Ensembl
Innerchr8:120503157..120519178hg18UCSC Ensembl
Innerchr8:120503157..120519178hg17UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3816022
hg1916022
hg1816022
hg1716022
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703407
Samples
Known GenesNOV
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527032
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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