A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4236291



Internal ID11518829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37215577..37215577hg38UCSC Ensembl
chr13:37789714..37789714hg19UCSC Ensembl
chr13:36687714..36687714hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38169
hg19169
hg18169
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1494306
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4236291
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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