A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907843



Internal ID22683053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106954411..106958425hg38UCSC Ensembl
chr11:106825137..106829151hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg384015
hg194015
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367312
Samples
Known GenesGUCY1A2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907843
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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