A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032021



Internal ID89052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14826049..14826068hg38UCSC Ensembl
chr10:14868048..14868067hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5535134
Supporting Variants
Samples
Known GenesCDNF
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032021
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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