A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714038



Internal ID137704
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 StatusS
Merged Variantsnsv5533377
Supporting Variants
Samples
Known GenesC17orf72, CD79B, CSHL1, GH1, ICAM2, SCN4A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714038
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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