A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587102



Internal ID21535662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:27003824..27003952hg38UCSC Ensembl
chr15:27248971..27249099hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17089267
SamplesNA19239
Known GenesGABRG3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587102
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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