A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5517229



Internal ID293655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76114400..76118425hg38UCSC Ensembl
chr17:74110481..74114506hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg384026
hg194026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714688
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5517229
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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