A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563328



Internal ID20936399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73409956..73410434hg38UCSC Ensembl
chr6:74119679..74120157hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38479
hg19479
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274083
Samples
Known GenesDDX43
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563328
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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