A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592473



Internal ID20965544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78084039..78084630hg38UCSC Ensembl
chr17:76080120..76080711hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243242
Samples
Known GenesTNRC6C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592473
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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