A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17429407



Internal ID22487277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:66675856..66707935hg38UCSC Ensembl
chr5:65971684..66003763hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3832080
hg1932080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896861
Supporting Variants
Samples
Known GenesMAST4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17429407
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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