A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900368



Internal ID22675509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:119708500..119713964hg38UCSC Ensembl
chr2:120466076..120471540hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg385465
hg195465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390108
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900368
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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