A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835538



Internal ID22610473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2099276..2102894hg38UCSC Ensembl
chr3:2140960..2144578hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg383619
hg193619
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17490894
Samples
Known GenesCNTN4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835538
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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