A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567199



Internal ID20940270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81461785..81462340hg38UCSC Ensembl
chr9:84076700..84077255hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7853n223
Supporting Variantsnssv18281145
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567199
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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