A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589083



Internal ID20962154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41997554..42000108hg38UCSC Ensembl
chr17:40149572..40152126hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg382555
hg192555
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242983
Samples
Known GenesDNAJC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589083
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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