A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611008



Internal ID16398417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39380149..39496421hg38UCSC Ensembl
Innerchr8:39237668..39353940hg19UCSC Ensembl
Innerchr8:39356825..39473097hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38116273
hg19116273
hg18116273
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12092n54
Supporting Variantsnssv1110573, nssv1110570, nssv1110565, nssv1110571, nssv1110569, nssv1110572, nssv1110568, nssv1110567, nssv1110566
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611008
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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