A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497823



Internal ID20871031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45667862..45749360hg38UCSC Ensembl
chr15:45960060..46041558hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3881499
hg1981499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179510
Samples
Known GenesSQRDL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497823
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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