A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764279



Internal ID20540139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60035640..60110885hg38UCSC Ensembl
chr17:58113001..58188246hg19UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg3875246
hg1975246
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv47n199
Supporting Variantsnssv16273228
Samples
Known GenesHEATR6, LOC645638, LOC653653, MIR4737
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764279
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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