A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884385



Internal ID22659367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:70813834..70830189hg38UCSC Ensembl
chr2:71040966..71057320hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg3816356
hg1916355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402284
Samples
Known GenesCLEC4F
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884385
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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