A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915073



Internal ID22690291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12023645..12023943hg38UCSC Ensembl
chr10:12065644..12065942hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366108
Samples
Known GenesUPF2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915073
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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