A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525059



Internal ID301235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15295043..15300789hg38UCSC Ensembl
chr17:15198360..15204106hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg385747
hg195747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17711679
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525059
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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