A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484206



Internal ID261624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100247808..100248329hg38UCSC Ensembl
chr10:102007565..102008086hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg38522
hg19522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038457
Samples
Known GenesCWF19L1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484206
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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