A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1035775



Internal ID11852214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:35966202..35966202hg38UCSC Ensembl
chrX:35984319..35984319hg19UCSC Ensembl
chrX:35894240..35894240hg18UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38216
hg19216
hg18216
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4153969
SamplesHuRef
Known GenesCXorf22
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1035775
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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