A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587425



Internal ID20960496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64700765..64701653hg38UCSC Ensembl
chr17:62696883..62697771hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg38889
hg19889
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3227n223
Supporting Variantsnssv18243298
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587425
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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