A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4086814



Internal ID11675061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63811411..63811411hg38UCSC Ensembl
chr10:65571171..65571171hg19UCSC Ensembl
chr10:65241177..65241177hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3852
hg1952
hg1852
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1738080
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4086814
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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