A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17615551



Internal ID21807598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9403551..9569788hg38UCSC Ensembl
chr12:9556147..9722384hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38166238
hg19166238
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6112153
Supporting Variants
Samples
Known GenesDDX12P
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17615551
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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