A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1159695



Internal ID12322818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36142679..36142679hg38UCSC Ensembl
chr13:36716816..36716816hg19UCSC Ensembl
chr13:35614816..35614816hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38293
hg19293
hg18293
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3782853
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1159695
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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