A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512763



Internal ID20886101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88919523..88965448hg38UCSC Ensembl
chr15:89462754..89508679hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3845926
hg1945926
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027014
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512763
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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