A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564500



Internal ID20937571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:122738281..122739344hg38UCSC Ensembl
chr6:123059426..123060489hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg381064
hg191064
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271128
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564500
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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