A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589436



Internal ID20962507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56839670..56840134hg38UCSC Ensembl
chr17:54917031..54917495hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38465
hg19465
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245948
Samples
Known GenesDGKE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589436
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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