A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383546



Internal ID21041099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:46741301..46741800hg38UCSC Ensembl
chr4:46743318..46743817hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117158
Samples
Known GenesCOX7B2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383546
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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