A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17091834



Internal ID21409420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75967684..75967737hg38UCSC Ensembl
chr17:73963765..73963818hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586983
Supporting Variants
SamplesHG00512
Known GenesACOX1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17091834
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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