A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5654881



Internal ID21603186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42518940..42518940hg38UCSC Ensembl
chr15:42811138..42811138hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38599
hg19599
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096048
SamplesHG01505
Known GenesSNAP23
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5654881
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer