A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581704



Internal ID20954775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32167498..32167887hg38UCSC Ensembl
chr17:30494517..30494906hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244417
Samples
Known GenesRHOT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581704
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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