A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466030



Internal ID21123583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62612193..62682304hg38UCSC Ensembl
chr11:62379665..62449776hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3870112
hg1970112
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196656
Samples
Known GenesB3GAT3, C11orf48, C11orf83, EML3, GANAB, INTS5, LOC102288414, METTL12, ROM1, SNORA57, UBXN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466030
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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