A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5441215



Internal ID219697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:209513478..209513548hg38UCSC Ensembl
chr2:210378202..210378272hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16928080
Samples
Known GenesMAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5441215
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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