A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548442



Internal ID20921628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:138706076..138722429hg38UCSC Ensembl
chr2:139463646..139479999hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3816354
hg1916354
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255957
Samples
Known GenesNXPH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548442
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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