A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217772



Internal ID20784812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:55917979..55918127hg38UCSC Ensembl
chr12:56311763..56311911hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581134
Supporting Variants
Samples
Known GenesWIBG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217772
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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