A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563419



Internal ID20936490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134890896..135471959hg38UCSC Ensembl
chr6:135212034..135793097hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38581064
hg19581064
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271959
Samples
Known GenesAHI1, ALDH8A1, HBS1L, MIR3662, MYB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563419
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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