A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580144



Internal ID20953215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:103869433..103869635hg38UCSC Ensembl
chr12:104263211..104263413hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232852
Samples
Known GenesGNN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580144
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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