A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583620



Internal ID20956691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74980155..74980934hg38UCSC Ensembl
chr16:75014053..75014832hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38780
hg19780
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241438
Samples
Known GenesWDR59
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583620
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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