A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1683473



Internal ID12499905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11283897..11284154hg38UCSC Ensembl
chr10:11325860..11326117hg19UCSC Ensembl
chr10:11365866..11366123hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38258
hg19258
hg18258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4351065
SamplesHuRef
Known GenesCELF2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1683473
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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