A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453649



Internal ID21111202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3800581..3821529hg38UCSC Ensembl
chr11:3821811..3842759hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3820949
hg1920949
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990577
Samples
Known GenesPGAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453649
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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