A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17138225



Internal ID21410675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42813993..42813993hg38UCSC Ensembl
chr5:42814095..42814095hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5629827
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17138225
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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