A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5507526



Internal ID284243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24326164..24326361hg38UCSC Ensembl
chr14:24795370..24795567hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17693435
Samples
Known GenesADCY4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5507526
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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