A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090166



Internal ID21407922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:94974965..94975017hg38UCSC Ensembl
chr15:95518194..95518246hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5597341
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090166
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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