A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562363



Internal ID20935434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104205223..104205772hg38UCSC Ensembl
chr7:103845671..103846220hg19UCSC Ensembl
Cytoband7q22.2
Allele length
AssemblyAllele length
hg38550
hg19550
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272205
Samples
Known GenesORC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562363
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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