A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1538999



Internal ID12702120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77430380..77430380hg38UCSC Ensembl
chr13:78004515..78004515hg19UCSC Ensembl
chr13:76902516..76902516hg18UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg3864
hg1964
hg1864
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4359348
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1538999
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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