A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5522075



Internal ID298349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56823567..56827424hg38UCSC Ensembl
chr17:54900928..54904785hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg383858
hg193858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17724818
Samples
Known GenesC17orf67
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5522075
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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