A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585341



Internal ID20958412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:55960561..55961248hg38UCSC Ensembl
chr12:56354345..56355032hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg38688
hg19688
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236212
Samples
Known GenesPMEL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585341
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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