A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17715100



Internal ID138766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:83210000..83247133hg38UCSC Ensembl
chr17:81157769..81194902hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3837134
hg1937134
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6144453
Supporting Variants
Samples
Known GenesFLJ43681
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17715100
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.028816


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