A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485929



Internal ID22543842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37263170..37265872hg38UCSC Ensembl
chr20:35891573..35894275hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg382703
hg192703
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5881136
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485929
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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