A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5507662



Internal ID284375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74050493..74050619hg38UCSC Ensembl
chr11:73761538..73761664hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17048359
Samples
Known GenesC2CD3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5507662
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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