A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588704



Internal ID20961775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74843220..74909355hg38UCSC Ensembl
chr16:74877118..74943253hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3866136
hg1966136
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2932n223
Supporting Variantsnssv18241432
Samples
Known GenesWDR59
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588704
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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