A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508113



Internal ID20881411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92844467..92868015hg38UCSC Ensembl
chr15:93387697..93411245hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3823549
hg1923549
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027320
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508113
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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