A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499051



Internal ID20872267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40875509..40891442hg38UCSC Ensembl
chr15:41167707..41183640hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3815934
hg1915934
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024226
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499051
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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