A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154338



Internal ID22084843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39372664..39529446hg38UCSC Ensembl
Outerchr8:39368830..39530780hg38UCSC Ensembl
Innerchr8:39230183..39386965hg19UCSC Ensembl
Outerchr8:39226349..39388299hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38161951
hg19161951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv285n97
Supporting Variantsnssv4004409, nssv4004410
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154338
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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