A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227974



Internal ID20795014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:7785423..7786128hg38UCSC Ensembl
chr12:7938019..7938724hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38706
hg19706
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581284
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227974
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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