A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512319



Internal ID20885652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43780306..43791141hg38UCSC Ensembl
chr15:44072504..44083339hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3810836
hg1910836
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023994
Samples
Known GenesSERF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512319
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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