A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463024



Internal ID21120577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118708275..118711044hg38UCSC Ensembl
chr11:118578984..118581753hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382770
hg192770
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986623
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463024
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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