A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563627



Internal ID20936698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128710940..128711407hg38UCSC Ensembl
chr7:128350994..128351461hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38468
hg19468
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273032
Samples
Known GenesFAM71F1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563627
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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