A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874432



Internal ID22649384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:28954682..29001208hg38UCSC Ensembl
chr21:30327004..30373529hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3846527
hg1946526
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488476
Samples
Known GenesLTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874432
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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