A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835365



Internal ID22610300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167582935..167609699hg38UCSC Ensembl
chr3:167300723..167327487hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3826765
hg1926765
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17487089
Samples
Known GenesWDR49
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835365
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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