A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746924



Internal ID20522940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70481420..70481487hg38UCSC Ensembl
chr4:71347137..71347204hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260331
Samples
Known GenesMUC7
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746924
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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