A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5441167



Internal ID219649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3306793..3307578hg38UCSC Ensembl
chr2:3310564..3311349hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38786
hg19786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16900970
Samples
Known GenesTSSC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5441167
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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