A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565623



Internal ID20938694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95536516..95537086hg38UCSC Ensembl
chr9:98298798..98299368hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38571
hg19571
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281528
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565623
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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