A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4199439



Internal ID11481977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86272075..86272075hg38UCSC Ensembl
chr11:85983117..85983117hg19UCSC Ensembl
chr11:85660765..85660765hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38901
hg19901
hg18901
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1712509
Supporting Variants
SamplesHuRef
Known GenesEED
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4199439
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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