A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610960



Internal ID16051683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39374115..39483882hg38UCSC Ensembl
Innerchr8:39231634..39341401hg19UCSC Ensembl
Innerchr8:39350791..39460558hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38109768
hg19109768
hg18109768
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12091n54
Supporting Variantsnssv1110033
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610960
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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