A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701090



Internal ID124756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74721605..74745146hg38UCSC Ensembl
chr15:75013946..75037487hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3823542
hg1923542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520955
Supporting Variants
Samples
Known GenesCYP1A1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701090
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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