A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17099614



Internal ID21504844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:82764855..82764855hg38UCSC Ensembl
chr17:80722731..80722731hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663129
Supporting Variants
SamplesNA19650
Known GenesTBCD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17099614
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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