A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509090



Internal ID285756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74051162..74052487hg38UCSC Ensembl
chr14:74517865..74519190hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381326
hg191326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17699263
Samples
Known GenesCCDC176
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509090
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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