A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15177033



Internal ID21315829
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3933846
Supporting Variants
SamplesHG002
Known GenesCEBPZ, CEBPZ-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15177033
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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