A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17144909



Internal ID21403959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24029451..24029451hg38UCSC Ensembl
chr6:24029679..24029679hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5639350
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17144909
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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