A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582703



Internal ID20955774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:49594996..49595728hg38UCSC Ensembl
chr17:47672358..47673090hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg38733
hg19733
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245141
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582703
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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