A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17145390



Internal ID21421299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6101631..6101631hg38UCSC Ensembl
chr5:6101744..6101744hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5637983
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17145390
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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