A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17124387



Internal ID21510491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32397296..32397296hg38UCSC Ensembl
chr3:32438788..32438788hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5608131
Supporting Variants
SamplesNA24385
Known GenesCMTM7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17124387
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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