A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591204



Internal ID20964275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:54934722..54936137hg38UCSC Ensembl
chr17:53012083..53013498hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg381416
hg191416
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245305
Samples
Known GenesTOM1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591204
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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