A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5891126



Internal ID22666160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:111081251..111111530hg38UCSC Ensembl
chr5:110416949..110447229hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3830280
hg1930281
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419226
Samples
Known GenesWDR36
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5891126
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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