A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611036



Internal ID16398445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39403008..39492792hg38UCSC Ensembl
Innerchr8:39260527..39350311hg19UCSC Ensembl
Innerchr8:39379684..39469468hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3889785
hg1989785
hg1889785
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12103n54
Supporting Variantsnssv1111157, nssv1111156
Samples
Known GenesADAM3A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611036
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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