A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591288



Internal ID21539863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39894052..39894324hg38UCSC Ensembl
chr15:40186253..40186525hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38273
hg19273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17097171
SamplesHG00171
Known GenesGPR176
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591288
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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