A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088467



Internal ID21450114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68246151..68246212hg38UCSC Ensembl
chr17:66242292..66242353hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5602580
Supporting Variants
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088467
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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