A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5996484



Internal ID21905827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168182401..168182605hg38UCSC Ensembl
chr4:169103552..169103756hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17544362
Samples
Known GenesANXA10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5996484
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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