A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3871459



Internal ID11890412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90267337..90267337hg38UCSC Ensembl
chr11:90000505..90000505hg19UCSC Ensembl
chr11:89640153..89640153hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38187
hg19187
hg18187
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1334387
Supporting Variants
SamplesHuRef
Known GenesDISC1FP1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3871459
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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