A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913898



Internal ID22689114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:99062431..99163809hg38UCSC Ensembl
chr11:98933161..99034540hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38101379
hg19101380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355130
Samples
Known GenesCNTN5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913898
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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