A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574021



Internal ID20947092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36417660..36418591hg38UCSC Ensembl
chr9:36417657..36418588hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38932
hg19932
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7696n223
Supporting Variantsnssv18280636
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574021
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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