A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571840



Internal ID20944911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:122791207..122792355hg38UCSC Ensembl
chr5:122126902..122128050hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg381149
hg191149
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266212
Samples
Known GenesSNX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571840
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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