A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096136



Internal ID21269202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:83064657..83068053hg38UCSC Ensembl
Innerchr15:83733409..83736805hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg383397
hg193397
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115647
Supporting Variants
Samplessample136
Known GenesBTBD1, MIR4515
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096136
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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