A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585015



Internal ID20958086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50734220..50734941hg38UCSC Ensembl
chr17:48811581..48812302hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg38722
hg19722
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3183n223
Supporting Variantsnssv18245170
Samples
Known GenesLUC7L3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585015
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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