A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222996



Internal ID20790036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:127935005..127935471hg38UCSC Ensembl
chr12:128419550..128420016hg19UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg38467
hg19467
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592802
Supporting Variants
Samples
Known GenesLINC00507
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222996
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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