A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915570



Internal ID22690788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61477122..61488222hg38UCSC Ensembl
chr11:61244594..61255694hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3811101
hg1911101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357735
Samples
Known GenesPPP1R32
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915570
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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