A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968271



Internal ID22743207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43334633..43334633hg38UCSC Ensembl
chr15:43626831..43626831hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17370188
Samples
Known GenesADAL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968271
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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