A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593743



Internal ID20966814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:79684376..79695567hg38UCSC Ensembl
chr17:77658237..77669491hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3811192
hg1911255
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243261
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593743
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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