A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095308



Internal ID21277872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87681084..87683716hg38UCSC Ensembl
Innerchr15:88224315..88226947hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg382633
hg192633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110447
Supporting Variants
Samplessample26
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095308
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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