A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869899



Internal ID22644834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3955446..3955495hg38UCSC Ensembl
chr2:4003036..4003085hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17395324
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869899
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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