A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749529



Internal ID20525560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73718255..73718310hg38UCSC Ensembl
chr15:74010596..74010651hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262072
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749529
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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