A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576286



Internal ID20949357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9403260..9570660hg38UCSC Ensembl
chr12:9555856..9723256hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38167401
hg19167401
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1395n223
Supporting Variantsnssv18231497
Samples
Known GenesDDX12P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576286
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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