A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5503973



Internal ID280784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35752578..35753338hg38UCSC Ensembl
chr15:36044779..36045539hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38761
hg19761
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701922
Samples
Known GenesDPH6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5503973
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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