A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460121



Internal ID21117674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76256187..76258804hg38UCSC Ensembl
chr11:75967231..75969848hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg382618
hg192618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994312
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460121
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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