A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4004442



Internal ID22066073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39378084..39529446hg38UCSC Ensembl
Outerchr8:39373140..39530780hg38UCSC Ensembl
Innerchr8:39235603..39386965hg19UCSC Ensembl
Outerchr8:39230659..39388299hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38157641
hg19157641
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154341
Supporting Variants
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4004442
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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