A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141392



Internal ID340588
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 StatusM
Merged Variants
Supporting Variantsnssv16952659
Samples
Known GenesCCSER1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141392
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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