A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1673449



Internal ID12489881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131680806..131680806hg38UCSC Ensembl
chr11:131550700..131550700hg19UCSC Ensembl
chr11:131055910..131055910hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38332
hg19332
hg18332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3662380
SamplesHuRef
Known GenesNTM
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1673449
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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