A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234669



Internal ID20801709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:57349379..57349567hg38UCSC Ensembl
chr12:57743162..57743350hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578084
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234669
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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