A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16952659



Internal ID35794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:90404103..90411309hg38UCSC Ensembl
chr4:91325254..91332460hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg387207
hg197207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141392
Supporting Variants
Samples
Known GenesCCSER1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16952659
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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