A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17390803



Internal ID22448673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36057187..36059609hg38UCSC Ensembl
chr20:34645109..34647531hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg382423
hg192423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5957179
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17390803
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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