A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183725



Internal ID20750765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72677391..72677728hg38UCSC Ensembl
chr15:72969732..72970069hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499765
Supporting Variants
Samples
Known GenesHIGD2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183725
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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