A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17122236



Internal ID21500456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:145805573..145805573hg38UCSC Ensembl
chr3:145523360..145523360hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5605899
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17122236
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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