A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111088



Internal ID22020321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:33684210..34380230hg38UCSC Ensembl
chr12:33837145..34533165hg19UCSC Ensembl
Cytoband12p11.1
Allele length
AssemblyAllele length
hg38696021
hg19696021
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611209
Samples
Known GenesALG10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111088
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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