A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594037



Internal ID20967108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9310308..9421532hg38UCSC Ensembl
chr12:9462904..9574128hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38111225
hg19111225
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1394n223
Supporting Variantsnssv18234925
Samples
Known GenesDDX12P, LOC642846
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594037
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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