A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034838



Internal ID19124059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:3449492..3556051hg38UCSC Ensembl
Innerchr8:3307014..3413573hg19UCSC Ensembl
Innerchr8:3294422..3400981hg18UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38106560
hg19106560
hg18106560
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3675326
Samples
Known GenesCSMD1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034838
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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