A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17710005



Internal ID133671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:2683111..2699111hg38UCSC Ensembl
chr17:2586405..2602405hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3816001
hg1916001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6145247
Supporting Variants
Samples
Known GenesCLUH, MIR6776, PAFAH1B1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17710005
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001134


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