A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5493832



Internal ID270998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17706452..17707954hg38UCSC Ensembl
chr10:17748451..17749953hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg381503
hg191503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030446
Samples
Known GenesSTAM
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5493832
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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