A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4184108



Internal ID11466646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:833811..833811hg38UCSC Ensembl
chr11:833811..833811hg19UCSC Ensembl
chr11:823811..823811hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1212776
Supporting Variants
SamplesHuRef
Known GenesCD151
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4184108
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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