A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5528790



Internal ID304832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15729628..15773956hg38UCSC Ensembl
chr17:15632942..15677270hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3844329
hg1944329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17711726
Samples
Known GenesCDRT15P2, TBC1D26
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5528790
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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