A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5494999



Internal ID272125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104320119..104320276hg38UCSC Ensembl
chr10:106079877..106080034hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038057
Samples
Known GenesITPRIP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5494999
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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