A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888919



Internal ID22663929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:224264771..224265053hg38UCSC Ensembl
chr2:225129488..225129770hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg38283
hg19283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392335
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888919
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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