A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17136881



Internal ID21439051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32208590..32208590hg38UCSC Ensembl
chr5:32208696..32208696hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5629648
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17136881
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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