A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904896



Internal ID22680075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206841615..206843390hg38UCSC Ensembl
chr2:207706339..207708114hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg381776
hg191776
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17395511
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904896
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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