A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589390



Internal ID20962461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:100828717..100829255hg38UCSC Ensembl
chr11:100699448..100699986hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38539
hg19539
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235598
Samples
Known GenesARHGAP42
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589390
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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