A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554713



Internal ID20927805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:159402363..159405546hg38UCSC Ensembl
chr2:160258874..160262057hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg383184
hg193184
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255356
Samples
Known GenesBAZ2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554713
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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