A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023264



Internal ID19112481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:127489522..127521674hg38UCSC Ensembl
Innerchr8:128501767..128533919hg19UCSC Ensembl
Innerchr8:128570949..128603101hg18UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3832153
hg1932153
hg1832153
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691518, nssv3691519, nssv3691517, nssv3691515, nssv3691516
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)nsv1023264
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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