A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17412991



Internal ID22470861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:140712153..140712448hg38UCSC Ensembl
chr4:141633307..141633602hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5905865
Supporting Variants
Samples
Known GenesTBC1D9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17412991
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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