A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541911



Internal ID20915179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:224398225..224398752hg38UCSC Ensembl
chr2:225262942..225263469hg19UCSC Ensembl
Cytoband2q36.2
Allele length
AssemblyAllele length
hg38528
hg19528
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257134
Samples
Known GenesFAM124B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541911
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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