A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17095728



Internal ID21458224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41382974..41383149hg38UCSC Ensembl
chr15:41675172..41675347hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5587730
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17095728
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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