A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485931



Internal ID22543844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37533309..37564876hg38UCSC Ensembl
chr20:36161711..36193278hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3831568
hg1931568
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869840
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485931
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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