A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460858



Internal ID21118411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62924826..62960156hg38UCSC Ensembl
chr11:62692298..62727628hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3835331
hg1935331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993242
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460858
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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