A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575876



Internal ID20948947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:57074328..57074972hg38UCSC Ensembl
chr12:57468111..57468755hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg38645
hg19645
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218975
Samples
Known GenesTMEM194A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575876
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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