A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510892



Internal ID20884215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89054202..89061298hg38UCSC Ensembl
chr15:89597433..89604529hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg387097
hg197097
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027022
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510892
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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