A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563521



Internal ID20936592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110826271..110826685hg38UCSC Ensembl
chr6:111147474..111147888hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267856
Samples
Known GenesAMD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563521
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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