A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574843



Internal ID20947914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:104774334..104775060hg38UCSC Ensembl
chr6:105222209..105222935hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38727
hg19727
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271038
Samples
Known GenesHACE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574843
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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