A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233177



Internal ID20800217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:30430537..30431329hg38UCSC Ensembl
chr12:30583470..30584262hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38793
hg19793
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579816
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233177
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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