A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899486



Internal ID22674616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:210940686..210940765hg38UCSC Ensembl
chr2:211805410..211805489hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17403594
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899486
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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