A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593896



Internal ID20966967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:40428631..40440736hg38UCSC Ensembl
chr17:38584883..38596988hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3812106
hg1912106
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242954
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593896
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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