A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739045



Internal ID20515017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149327061..149327302hg38UCSC Ensembl
chr5:148706624..148706865hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38242
hg19242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283760
Samples
Known GenesAFAP1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739045
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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