A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5937868



Internal ID22713242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:57879654..57879868hg38UCSC Ensembl
chr12:58273437..58273651hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357772
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5937868
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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