A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499765



Internal ID20872988
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 StatusM
Merged Variants
Supporting Variantsnssv18183725
Samples
Known GenesHIGD2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499765
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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