A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538479



Internal ID20911796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:160395412..160396540hg38UCSC Ensembl
chr2:161251923..161253051hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg381129
hg191129
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255387
Samples
Known GenesRBMS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538479
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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