A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025929



Internal ID19115146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:40441510..40492672hg38UCSC Ensembl
Innerchr8:40299029..40350191hg19UCSC Ensembl
Innerchr8:40418186..40469348hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3851163
hg1951163
hg1851163
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3687244
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)nsv1025929
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