A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17117185



Internal ID21421944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59442200..59442200hg38UCSC Ensembl
chr20:58017255..58017255hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668780
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17117185
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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