A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5527698



Internal ID303784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85406376..85411008hg38UCSC Ensembl
chr15:85949607..85954239hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg384633
hg194633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702268
Samples
Known GenesAKAP13
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5527698
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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