A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485664



Internal ID263048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15121057..15124163hg38UCSC Ensembl
chr10:15163056..15166162hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg383107
hg193107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17032054
Samples
Known GenesNMT2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485664
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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