A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460953



Internal ID238919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3774407..3778769hg38UCSC Ensembl
chr6:3774641..3779003hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg384363
hg194363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979887
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460953
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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