A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739150



Internal ID20515122
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 StatusM
Merged Variants
Supporting Variantsnssv16273124
Samples
Known GenesNBAS
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739150
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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