A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5507836



Internal ID284545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51359531..51361207hg38UCSC Ensembl
chr14:51826249..51827925hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg381677
hg191677
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17696172
Samples
Known GenesLINC00640
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5507836
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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