A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903573



Internal ID22678742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:114970459..114983837hg38UCSC Ensembl
chr2:115728036..115741414hg19UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg3813379
hg1913379
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17395973
Samples
Known GenesDPP10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903573
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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