A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918896



Internal ID22694118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62029157..62068495hg38UCSC Ensembl
chr11:61796629..61835967hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3839339
hg1939339
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357292
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918896
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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