A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591830



Internal ID20964901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121926536..121926868hg38UCSC Ensembl
chr12:122364442..122364774hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225005
Samples
Known GenesWDR66
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591830
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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