A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281556



Internal ID20490774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25999969..26000059hg38UCSC Ensembl
chr15:26245116..26245206hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744381
Supporting Variants
Samples
Known GenesLOC100128714
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281556
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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