A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034285



Internal ID19123507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:113214885..113265812hg38UCSC Ensembl
Innerchr8:114227114..114278041hg19UCSC Ensembl
Innerchr8:114296290..114347217hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3850928
hg1950928
hg1850928
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691308
Samples
Known GenesCSMD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034285
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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