A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090268



Internal ID21485001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63456621..63456621hg38UCSC Ensembl
chr17:61533982..61533982hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655130
Supporting Variants
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090268
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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