A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472514



Internal ID21130067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110089101..110100300hg38UCSC Ensembl
chr11:109959827..109971025hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3811200
hg1911199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180335
Samples
Known GenesZC3H12C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472514
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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