A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1649942



Internal ID12813061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128868092..128868092hg38UCSC Ensembl
chr11:128737987..128737987hg19UCSC Ensembl
chr11:128243197..128243197hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg382307
hg192307
hg182307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4099511
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1649942
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