A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5504198



Internal ID281006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112766292..112767193hg38UCSC Ensembl
chr10:114526051..114526952hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038172
Samples
Known GenesVTI1A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5504198
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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