A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3892494



Internal ID11869377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46384783..46384783hg38UCSC Ensembl
chrX:46244218..46244218hg19UCSC Ensembl
chrX:46129162..46129162hg18UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3858
hg1958
hg1858
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1289837
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3892494
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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