A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662331



Internal ID21610636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41949051..41949051hg38UCSC Ensembl
chr15:42241249..42241249hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17098021
SamplesNA19983
Known GenesEHD4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662331
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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