A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5989905



Internal ID21899248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:75154434..75154488hg38UCSC Ensembl
chr2:75381560..75381614hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17523676
Samples
Known GenesTACR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5989905
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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