A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1220296



Internal ID12383419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27160512..27161159hg38UCSC Ensembl
chr1:27487003..27487650hg19UCSC Ensembl
chr1:27359590..27360237hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38648
hg19648
hg18648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3949051
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1220296
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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