A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4267817



Internal ID11203669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131680444..131680444hg38UCSC Ensembl
chr11:131550338..131550338hg19UCSC Ensembl
chr11:131055548..131055548hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38658
hg19658
hg18658
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1144589
Supporting Variants
SamplesHuRef
Known GenesNTM
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4267817
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer