A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1386391



Internal ID12549513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:47132605..47132691hg38UCSC Ensembl
chr15:47424803..47424889hg19UCSC Ensembl
chr15:45212095..45212181hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3887
hg1987
hg1887
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3684410
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1386391
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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