A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599440



Internal ID20972511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37248023..37249292hg38UCSC Ensembl
chr20:35876426..35877695hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg381270
hg191270
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4456n223
Supporting Variantsnssv18254352
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599440
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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