A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997880



Internal ID21907223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70481290..70481358hg38UCSC Ensembl
chr4:71347007..71347075hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547748
Samples
Known GenesMUC7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997880
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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