A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17125482



Internal ID21453419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194634644..194635901hg38UCSC Ensembl
chr3:194355373..194356630hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381258
hg191258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574082
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17125482
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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