A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108976



Internal ID22018209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9199258..9594739hg38UCSC Ensembl
chr12:9351854..9747335hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38395482
hg19395482
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609395
Samples
Known GenesA2MP1, DDX12P, LINC00987, LOC642846, MIR1244-1, MIR1244-2, MIR1244-3, PZP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108976
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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