A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17396142



Internal ID22454012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1523416..1523908hg38UCSC Ensembl
chr20:1504062..1504554hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38493
hg19493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5937561
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17396142
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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