A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894850



Internal ID22669926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:176934680..176938013hg38UCSC Ensembl
chr2:177799408..177802741hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg383334
hg193334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390841
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894850
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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