A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831641



Internal ID22606576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:152324674..152354304hg38UCSC Ensembl
chr2:153181188..153210818hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg3829631
hg1929631
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17487806
Samples
Known GenesFMNL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831641
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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