A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16273124



Internal ID20482342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15481529..15481630hg38UCSC Ensembl
chr2:15621653..15621754hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739150
Supporting Variants
Samples
Known GenesNBAS
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16273124
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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