A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590202



Internal ID20963273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:57033744..57034679hg38UCSC Ensembl
chr12:57427528..57428463hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg38936
hg19936
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1549n223
Supporting Variantsnssv18231529
Samples
Known GenesMYO1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590202
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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