A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485969



Internal ID22543882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40089397..40113805hg38UCSC Ensembl
chr20:38718038..38742446hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3824409
hg1924409
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876398
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485969
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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