A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258062



Internal ID20825102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:47793332..47794275hg38UCSC Ensembl
chr2:48020471..48021414hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38944
hg19944
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551245
Supporting Variants
Samples
Known GenesMSH6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258062
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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