A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1401879



Internal ID12565002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70585510..70585751hg38UCSC Ensembl
chr15:70877849..70878090hg19UCSC Ensembl
chr15:68664903..68665144hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38242
hg19242
hg18242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3851952
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1401879
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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