A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701086



Internal ID124752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74675383..74678474hg38UCSC Ensembl
chr15:74967724..74970815hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg383092
hg193092
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5525170
Supporting Variants
Samples
Known GenesEDC3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701086
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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