A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963977



Internal ID22738912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:19695205..19703795hg38UCSC Ensembl
chr20:19675849..19684439hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg388591
hg198591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17404661
Samples
Known GenesSLC24A3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963977
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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