A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504434



Internal ID20877695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:87192975..87206206hg38UCSC Ensembl
chr15:87736206..87749437hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3813232
hg1913232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025880
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504434
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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