A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1462891



Internal ID12626013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155016518..155016518hg38UCSC Ensembl
chr6:155337652..155337652hg19UCSC Ensembl
chr6:155379344..155379344hg18UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3855
hg1955
hg1855
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4296745
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1462891
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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