A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569256



Internal ID20942327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125402458..125516539hg38UCSC Ensembl
chr6:125723604..125837685hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38114082
hg19114082
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271168
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569256
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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