A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5554357



Internal ID327547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44378784..44381820hg38UCSC Ensembl
chr10:44874232..44877268hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg383037
hg193037
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17034953
Samples
Known GenesCXCL12
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5554357
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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