A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610968



Internal ID16398377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39375062..39507199hg38UCSC Ensembl
Innerchr8:39232581..39364718hg19UCSC Ensembl
Innerchr8:39351738..39483875hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38132138
hg19132138
hg18132138
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12093n54
Supporting Variantsnssv1110057, nssv1110056
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610968
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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