A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405946



Internal ID21063499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:66910724..66912240hg38UCSC Ensembl
chr5:66206552..66208068hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg381517
hg191517
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133931
Samples
Known GenesMAST4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405946
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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