A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5891901



Internal ID22666944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206074839..206074938hg38UCSC Ensembl
chr2:206939563..206939662hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17395719
Samples
Known GenesINO80D
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5891901
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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