A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560657



Internal ID20933728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:135033164..135139346hg38UCSC Ensembl
chr6:135354302..135460484hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38106183
hg19106183
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271965
Samples
Known GenesHBS1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560657
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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