A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568099



Internal ID20941170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:147739529..147739811hg38UCSC Ensembl
chr6:148060665..148060947hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38283
hg19283
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273230
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568099
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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