A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1069714



Internal ID11886153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:49689781..49689781hg38UCSC Ensembl
chrX:49454384..49454384hg19UCSC Ensembl
chrX:49341313..49341313hg18UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38114
hg19114
hg18114
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4118262
SamplesHuRef
Known GenesPAGE1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1069714
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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