A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852148



Internal ID22627083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:99154400..99155499hg38UCSC Ensembl
chr11:99025131..99026230hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465307, nssv17451138
Samples
Known GenesCNTN5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852148
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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