A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573309



Internal ID20946380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101183332..101183973hg38UCSC Ensembl
chr8:102195560..102196201hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38642
hg19642
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7440n223
Supporting Variantsnssv18275912
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573309
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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