A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555128



Internal ID20928217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202946631..202947711hg38UCSC Ensembl
chr2:203811354..203812434hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg381081
hg191081
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257777
Samples
Known GenesCARF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555128
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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