A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3933846



Internal ID21353915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:37202656..37202705hg38UCSC Ensembl
chr2:37429799..37429848hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15177033
SamplesHG002
Known GenesCEBPZ, CEBPZ-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3933846
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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