A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102296



Internal ID22011532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:30248337..30348815hg38UCSC Ensembl
chr12:30401270..30501748hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38100479
hg19100479
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611766
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102296
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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