A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14085852



Internal ID21284302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39487501..39494202hg38UCSC Ensembl
Innerchr8:39345020..39351721hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg386702
hg196702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114848
Supporting Variants
Samplessample36
Known GenesADAM3A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14085852
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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