A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5522100



Internal ID298373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75349325..75349376hg38UCSC Ensembl
chr17:73345406..73345457hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714630
Samples
Known GenesGRB2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5522100
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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