A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5528645



Internal ID304694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9754209..9757360hg38UCSC Ensembl
chr17:9657526..9660677hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg383152
hg193152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17711355
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5528645
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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