A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506936



Internal ID20880224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67846887..67866154hg38UCSC Ensembl
chr15:68139225..68158492hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3819268
hg1919268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025479
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506936
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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