A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506052



Internal ID20879327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49007765..49008119hg38UCSC Ensembl
chr15:49299962..49300316hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024760
Samples
Known GenesSECISBP2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506052
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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