A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559540



Internal ID20932611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66440715..66442165hg38UCSC Ensembl
chr7:65905702..65907152hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg381451
hg191451
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274292
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559540
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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