A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234570



Internal ID20801610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:30685475..30685637hg38UCSC Ensembl
chr12:30838409..30838571hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576543
Supporting Variants
Samples
Known GenesIPO8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234570
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00019


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