A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539800



Internal ID20913095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:165515278..165516132hg38UCSC Ensembl
chr2:166371788..166372642hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38855
hg19855
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255831
Samples
Known GenesCSRNP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539800
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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