A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001253



Internal ID21910596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77042405..77042553hg38UCSC Ensembl
chr5:76338230..76338378hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555812
Samples
Known GenesAGGF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001253
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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