A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5529561



Internal ID305574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64935344..64936618hg38UCSC Ensembl
chr15:65227542..65228816hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381275
hg191275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704241
Samples
Known GenesANKDD1A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5529561
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer