A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598103



Internal ID20971174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:46630794..46643794hg38UCSC Ensembl
chr20:45259433..45272433hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3813001
hg1913001
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252150
Samples
Known GenesSLC13A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598103
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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