A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363471



Internal ID21021024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48851843..48858505hg38UCSC Ensembl
chr3:48889276..48895938hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg386663
hg196663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102000
Samples
Known GenesSLC25A20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363471
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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