A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611041



Internal ID16398450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39403008..39546375hg38UCSC Ensembl
Innerchr8:39260527..39403894hg19UCSC Ensembl
Innerchr8:39379684..39523051hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38143368
hg19143368
hg18143368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12095n54
Supporting Variantsnssv1111175
Samples
Known GenesADAM3A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611041
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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