A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564952



Internal ID20938023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72047663..72050481hg38UCSC Ensembl
chr9:74662579..74665397hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382819
hg192819
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280899
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564952
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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