A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593672



Internal ID20966743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60019455..60127187hg38UCSC Ensembl
chr17:58096816..58204548hg19UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg38107733
hg19107733
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242431
Samples
Known GenesHEATR6, LOC645638, LOC653653, MIR4737
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593672
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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