A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831860



Internal ID22606795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:204991214..205027457hg38UCSC Ensembl
chr2:205855937..205892180hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg3836244
hg1936244
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482012
Samples
Known GenesPARD3B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831860
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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