A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17486041



Internal ID22543954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:44669037..44675239hg38UCSC Ensembl
chr20:43297678..43303880hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg386203
hg196203
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5885791
Supporting Variants
Samples
Known GenesLOC79015
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17486041
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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