A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17127726



Internal ID21412700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23643946..23643946hg38UCSC Ensembl
chr3:23685437..23685437hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5609341
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17127726
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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