A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1720208



Internal ID12883326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115403085..115403085hg38UCSC Ensembl
chrX:114637659..114637659hg19UCSC Ensembl
chrX:114543915..114543915hg18UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38144
hg19144
hg18144
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3750654
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1720208
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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