A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093227



Internal ID21452561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75712783..75714084hg38UCSC Ensembl
chr15:76005124..76006425hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg381302
hg191302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588308
Supporting Variants
SamplesHG01596
Known GenesCSPG4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093227
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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