A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236478



Internal ID20803518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121317006..121637833hg38UCSC Ensembl
chr12:121754809..122075739hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38320828
hg19320931
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581635
Supporting Variants
Samples
Known GenesANAPC5, KDM2B, MIR7107, ORAI1, RNF34
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236478
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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