A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539139



Internal ID20912446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:24184260..24185018hg38UCSC Ensembl
chr2:24407129..24407887hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38759
hg19759
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258102
Samples
Known GenesFAM228A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539139
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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