A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17158089



Internal ID21426791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:80557295..80557295hg38UCSC Ensembl
chr6:81267012..81267012hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5642256
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17158089
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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