A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17091129



Internal ID21450043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68245685..68245685hg38UCSC Ensembl
chr17:66241826..66241826hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5645959
Supporting Variants
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17091129
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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