A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5648109



Internal ID21596414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39894052..39894052hg38UCSC Ensembl
chr15:40186253..40186253hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17090643, nssv17093951
SamplesNA19238, HG00731
Known GenesGPR176
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5648109
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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