A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17080857



Internal ID21490228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76310157..76310329hg38UCSC Ensembl
chr17:74306238..74306410hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5598527
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17080857
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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