A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869539



Internal ID22644474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:102905057..102918703hg38UCSC Ensembl
chr2:103521515..103535161hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg3813647
hg1913647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17405043
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869539
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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