A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17724819



Internal ID148485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56826620..56827436hg38UCSC Ensembl
chr17:54903981..54904797hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38817
hg19817
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528412
Supporting Variants
Samples
Known GenesC17orf67
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17724819
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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