A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16262528



Internal ID20471746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40037606..40037692hg38UCSC Ensembl
chr15:40329807..40329893hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733441
Supporting Variants
Samples
Known GenesSRP14
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16262528
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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