A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097553



Internal ID21275151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:83901682..83908210hg38UCSC Ensembl
Innerchr15:84570434..84576962hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg386529
hg196529
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116881
Supporting Variants
Samplessample218
Known GenesADAMTSL3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097553
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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