A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156388



Internal ID15531620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:144007080..144224185hg38UCSC Ensembl
Innerchr8:145081248..145279088hg19UCSC Ensembl
Innerchr8:145153236..145351076hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38217106
hg19197841
hg18197841
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612915
Supporting Variants
SamplesHGDP01177
Known GenesCYC1, EXOSC4, FAM203A, GPAA1, KIAA1875, MAF1, MIR6846, MIR6847, MROH1, OPLAH, SHARPIN, SPATC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156388
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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