A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5833264



Internal ID22608199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:45246292..45297805hg38UCSC Ensembl
chr2:45473431..45524944hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3851514
hg1951514
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486109
Samples
Known GenesLINC01121
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5833264
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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