A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5523702



Internal ID299927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58730462..58730912hg38UCSC Ensembl
chr17:56807823..56808273hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38451
hg19451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17713829
Samples
Known GenesRAD51C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5523702
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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