A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17127063



Internal ID21403174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:152047141..152047580hg38UCSC Ensembl
chr3:151764930..151765369hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38440
hg19440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5572823
Supporting Variants
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17127063
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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