A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16264804



Internal ID20474022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25634211..25634262hg38UCSC Ensembl
chr2:25857080..25857131hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746735
Supporting Variants
Samples
Known GenesDTNB
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16264804
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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