A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564677



Internal ID20937748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37475855..37476715hg38UCSC Ensembl
chr9:37475852..37476712hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38861
hg19861
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280675
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564677
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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