A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893095



Internal ID22668152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:166845069..166847403hg38UCSC Ensembl
chr2:167701579..167703913hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg382335
hg192335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17396192
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893095
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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