A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505722



Internal ID20878995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90841808..90852022hg38UCSC Ensembl
chr15:91385038..91395252hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3810215
hg1910215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027395
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505722
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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