A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883568



Internal ID22658549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:84906117..84906387hg38UCSC Ensembl
chr2:85133241..85133511hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17408368
Samples
Known GenesTMSB10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883568
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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