A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581635



Internal ID20954706
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 StatusM
Merged Variants
Supporting Variantsnssv18236478
Samples
Known GenesANAPC5, KDM2B, MIR7107, ORAI1, RNF34
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581635
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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