A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855614



Internal ID22630549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64326081..64344287hg38UCSC Ensembl
chr11:64093553..64111759hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3818207
hg1918207
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460437
Samples
Known GenesCCDC88B, MIR7155
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855614
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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