A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5535134



Internal ID310829
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 StatusM
Merged Variants
Supporting Variantsnssv17032021
Samples
Known GenesCDNF
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5535134
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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