A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218584



Internal ID20785624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:55833857..55834533hg38UCSC Ensembl
chr12:56227641..56228317hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg38677
hg19677
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594510
Supporting Variants
Samples
Known GenesTMEM198B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218584
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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