A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905875



Internal ID22681068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:207186686..207187390hg38UCSC Ensembl
chr2:208051410..208052114hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38705
hg19705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399830
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905875
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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