A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580417



Internal ID20953488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95476488..95477279hg38UCSC Ensembl
chr12:95870264..95871055hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38792
hg19792
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222160
Samples
Known GenesMETAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580417
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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