A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594435



Internal ID20967506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65620540..65622946hg38UCSC Ensembl
chr17:63616658..63619064hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg382407
hg192407
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3230n223
Supporting Variantsnssv18245998
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594435
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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