A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933203



Internal ID22708512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:45056218..45056373hg38UCSC Ensembl
chr12:45450001..45450156hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365151
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933203
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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