A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573212



Internal ID20946283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107986569..107987151hg38UCSC Ensembl
chr6:108307773..108308355hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269822
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573212
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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