A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594967



Internal ID20968038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:43900620..43901567hg38UCSC Ensembl
chr12:44294423..44295370hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38948
hg19948
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225180
Samples
Known GenesTMEM117
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594967
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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