A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1409369



Internal ID12572491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110701702..110702066hg38UCSC Ensembl
chr12:111139507..111139871hg19UCSC Ensembl
chr12:109623890..109624254hg18UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38365
hg19365
hg18365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4120635
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1409369
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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