A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899641



Internal ID22674772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:74353677..74357975hg38UCSC Ensembl
chr3:74402828..74407126hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg384299
hg194299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425965
Samples
Known GenesCNTN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899641
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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