A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17085828



Internal ID21511203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65326077..65326472hg38UCSC Ensembl
chr15:65618415..65618810hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5597180
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17085828
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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