A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355293



Internal ID22580962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:55832069..55833939hg38UCSC Ensembl
chr12:56225853..56227723hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg381871
hg191871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5934341
Supporting Variants
Samples
Known GenesTMEM198B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355293
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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