A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553128



Internal ID20926237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38351556..38352124hg38UCSC Ensembl
chr2:38578698..38579266hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg38569
hg19569
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260197
Samples
Known GenesATL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553128
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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