A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5833684



Internal ID22608619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:64455203..64456219hg38UCSC Ensembl
chr2:64682337..64683353hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg381017
hg191017
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17487595
Samples
Known GenesLGALSL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5833684
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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