A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5491100



Internal ID268344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31562886..31578489hg38UCSC Ensembl
chr10:31851814..31867417hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3815604
hg1915604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17031437
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5491100
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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