A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611044



Internal ID16398453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39405020..39529660hg38UCSC Ensembl
Innerchr8:39262539..39387179hg19UCSC Ensembl
Innerchr8:39381696..39506336hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38124641
hg19124641
hg18124641
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12094n54
Supporting Variantsnssv1111180, nssv1111179
Samples
Known GenesADAM3A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611044
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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