A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887332



Internal ID22662324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14201799..14202997hg38UCSC Ensembl
chr21:15574120..15575318hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg381199
hg191199
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17487966
Samples
Known GenesLIPI
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887332
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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