A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893207



Internal ID22668265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:66606859..66606924hg38UCSC Ensembl
chr5:65902687..65902752hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417580
Samples
Known GenesMAST4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893207
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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