A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497680



Internal ID20870888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45684212..45686387hg38UCSC Ensembl
chr15:45976410..45978585hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg382176
hg192176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024626
Samples
Known GenesSQRDL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497680
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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