A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568629



Internal ID20941700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:124738085..124739105hg38UCSC Ensembl
chr6:125059231..125060251hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg381021
hg191021
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271160
Samples
Known GenesNKAIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568629
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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