A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565972



Internal ID20939043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:140894235..141114154hg38UCSC Ensembl
chr6:141215372..141435291hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38219920
hg19219920
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272534
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565972
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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