A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17715105



Internal ID138771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:83214950..83223566hg38UCSC Ensembl
chr17:81162719..81171335hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg388617
hg198617
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6145936
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17715105
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.023282


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