A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533377



Internal ID309266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63906475..64023565hg38UCSC Ensembl
chr17:61983835..62100925hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38117091
hg19117091
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714038
Samples
Known GenesC17orf72, CD79B, CSHL1, GH1, ICAM2, SCN4A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533377
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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