A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271984



Internal ID20481202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74454846..74454992hg38UCSC Ensembl
chr15:74747187..74747333hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739610
Supporting Variants
Samples
Known GenesUBL7
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271984
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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