A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196656



Internal ID20763696
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 StatusS
Merged Variantsnsv6466030
Supporting Variants
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)nssv18196656
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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