A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159373



Internal ID21472073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:23661023..23661023hg38UCSC Ensembl
chr6:23661251..23661251hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5630718
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159373
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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