A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834806



Internal ID22609741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179070926..179073043hg38UCSC Ensembl
chr3:178788714..178790831hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg382118
hg192118
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17489720
Samples
Known GenesZMAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834806
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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