A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1105055



Internal ID12268179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73120244..73120244hg38UCSC Ensembl
chr13:73694381..73694381hg19UCSC Ensembl
chr13:72592382..72592382hg18UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg3851
hg1951
hg1851
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3610651
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1105055
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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