A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232076



Internal ID20799116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:101758237..101759108hg38UCSC Ensembl
chr12:102152015..102152886hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg38872
hg19872
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591672
Supporting Variants
Samples
Known GenesGNPTAB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232076
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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