A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5535421



Internal ID311059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78328736..78328736hg38UCSC Ensembl
chr15:78621078..78621078hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702186
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5535421
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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