A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880078



Internal ID22655048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:110101062..110104078hg38UCSC Ensembl
chr2:110858639..110861655hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg383017
hg193017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17394299
Samples
Known GenesMALL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880078
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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