A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973812



Internal ID22748747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:76310068..76310068hg38UCSC Ensembl
chr15:76602409..76602409hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388180
Samples
Known GenesETFA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973812
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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