A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546438



Internal ID20919657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202942099..202943373hg38UCSC Ensembl
chr2:203806822..203808096hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg381275
hg191275
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257775
Samples
Known GenesCARF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546438
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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