A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17083732



Internal ID21504924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75701222..75701287hg38UCSC Ensembl
chr15:75993563..75993628hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588961
Supporting Variants
SamplesNA19650
Known GenesCSPG4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17083732
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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