A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17127162



Internal ID21454301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:152695012..152695012hg38UCSC Ensembl
chr3:152412801..152412801hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg384889
hg194889
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5621766
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17127162
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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