A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17136729



Internal ID21469315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:31191074..31191074hg38UCSC Ensembl
chr5:31191181..31191181hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38410
hg19410
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5641438
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17136729
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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