A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17081129



Internal ID21450379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78631966..78631966hg38UCSC Ensembl
chr17:76628048..76628048hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5649476
Supporting Variants
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17081129
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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