A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4004460



Internal ID22066091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39378084..39531605hg38UCSC Ensembl
Outerchr8:39373140..39537590hg38UCSC Ensembl
Innerchr8:39235603..39389124hg19UCSC Ensembl
Outerchr8:39230659..39395109hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38164451
hg19164451
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154342
Supporting Variants
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4004460
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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