A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232955



Internal ID20799995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:42521445..42522019hg38UCSC Ensembl
chr12:42915247..42915821hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38575
hg19575
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585743
Supporting Variants
Samples
Known GenesPRICKLE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232955
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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