A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17997801



Internal ID20564841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121712401..121712900hg38UCSC Ensembl
chr12:122150307..122150806hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6488129
Supporting Variants
Samples
Known GenesTMEM120B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17997801
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.08814


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