A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17137836



Internal ID21418018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195047788..195047788hg38UCSC Ensembl
chr3:194768517..194768517hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5611698
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17137836
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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