A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092710



Internal ID21431771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:29949853..29949996hg38UCSC Ensembl
chr15:30242056..30242199hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5595745
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092710
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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