A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592711



Internal ID20965782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25003253..25003573hg38UCSC Ensembl
chr16:25014574..25014894hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242739
Samples
Known GenesARHGAP17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592711
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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