A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731407



Internal ID20507328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149111668..149111733hg38UCSC Ensembl
chr5:148491231..148491296hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292014
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731407
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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