A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17146780



Internal ID21498358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:60282281..60282281hg38UCSC Ensembl
chr8:61194840..61194840hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5624765
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17146780
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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