A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582839



Internal ID20955910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42330139..42332845hg38UCSC Ensembl
chr17:40482157..40484863hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg382707
hg192707
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3116n223
Supporting Variantsnssv18242997
Samples
Known GenesSTAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582839
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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