A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1121726



Internal ID12284849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26724010..26724059hg38UCSC Ensembl
chr13:27298147..27298196hg19UCSC Ensembl
chr13:26196147..26196196hg18UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3695501
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1121726
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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