A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593150



Internal ID20966221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81630361..81630883hg38UCSC Ensembl
chr17:79597387..79597909hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38523
hg19523
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243900
Samples
Known GenesNPLOC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593150
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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