A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107994



Internal ID22017229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:17701486..17805863hg38UCSC Ensembl
chr12:17854420..17958797hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38104378
hg19104378
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608030
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107994
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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