A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882204



Internal ID22657181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:104404014..104404558hg38UCSC Ensembl
chr2:105020472..105021016hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg38545
hg19545
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389813
Samples
Known GenesLOC100287010
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882204
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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