A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5527602



Internal ID303695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72184658..72184722hg38UCSC Ensembl
chr15:72476999..72477063hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702426
Samples
Known GenesGRAMD2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5527602
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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