A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221070



Internal ID20788110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8640763..8641724hg38UCSC Ensembl
chr12:8793359..8794320hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38962
hg19962
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576198
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221070
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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