A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093592



Internal ID21282012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15181865..15264386hg38UCSC Ensembl
Innerchr4:15183489..15266010hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3882522
hg1982522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115802
Supporting Variants
Samplessample320
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093592
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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