A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086952



Internal ID21291803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39375671..39454268hg38UCSC Ensembl
Innerchr8:39233190..39311787hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3878598
hg1978598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110925
Supporting Variants
Samplessample79
Known GenesADAM3A, ADAM5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086952
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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