A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956152



Internal ID22731344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:16149891..16150219hg38UCSC Ensembl
chr21:17522211..17522539hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17401009
Samples
Known GenesLINC00478
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956152
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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