A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263918



Internal ID20473136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74837492..74837543hg38UCSC Ensembl
chr15:75129833..75129884hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739090
Supporting Variants
Samples
Known GenesULK3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263918
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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