A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5472805



Internal ID250507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:52051823..52051905hg38UCSC Ensembl
chr4:52917989..52918071hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16950037
Samples
Known GenesSPATA18
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5472805
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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