A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611009



Internal ID16398418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39380149..39498641hg38UCSC Ensembl
Innerchr8:39237668..39356160hg19UCSC Ensembl
Innerchr8:39356825..39475317hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38118493
hg19118493
hg18118493
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12092n54
Supporting Variantsnssv1110574
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611009
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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