A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874890



Internal ID22649844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27512067..27512362hg38UCSC Ensembl
chr2:27734934..27735229hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17406403
Samples
Known GenesGCKR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874890
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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