A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995520



Internal ID21904863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155670447..155691067hg38UCSC Ensembl
chr4:156591599..156612219hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3820621
hg1920621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551424
Samples
Known GenesGUCY1A3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995520
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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