A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17138290



Internal ID21445160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188015036..188016973hg38UCSC Ensembl
chr3:187732824..187734761hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg381938
hg191938
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574844
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17138290
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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