A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593728



Internal ID20966799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62498491..62499641hg38UCSC Ensembl
chr17:60575852..60577002hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg381151
hg191151
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242585
Samples
Known GenesTLK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593728
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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