A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17029355



Internal ID87262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:2646620..3092107hg38UCSC Ensembl
chr10:2688812..3134299hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38445488
hg19445488
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142627
Supporting Variants
Samples
Known GenesPFKP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17029355
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001874


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