A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5595311



Internal ID21543915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92487988..92488592hg38UCSC Ensembl
chr15:93031218..93031822hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38605
hg19605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17080395
SamplesNA19239
Known GenesC15orf32
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5595311
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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