A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17097315



Internal ID21492677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95211315..95211368hg38UCSC Ensembl
chr15:95754544..95754597hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5600573
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17097315
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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