A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492283



Internal ID269500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18771898..18980140hg38UCSC Ensembl
chr10:19060827..19269069hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38208243
hg19208243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17032601
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492283
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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