A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086091



Internal ID21502719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:80217586..80217638hg38UCSC Ensembl
chr17:78191385..78191437hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5589196
Supporting Variants
SamplesNA19239
Known GenesSGSH
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086091
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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