A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568079



Internal ID20941150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138581487..138582058hg38UCSC Ensembl
chr6:138902624..138903195hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38572
hg19572
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272463
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568079
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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