A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179794



Internal ID20746834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50100747..50151178hg38UCSC Ensembl
chr15:50392944..50443375hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3850432
hg1950432
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510087
Supporting Variants
Samples
Known GenesATP8B4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179794
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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