A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555522



Internal ID20928608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:226169727..226177472hg38UCSC Ensembl
chr1:226357428..226365173hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg387746
hg197746
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249438
Samples
Known GenesACBD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555522
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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