A curated catalogue of human genomic structural variation




Variant Details

Variant: esv990696



Internal ID7076827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:44437968..44446460hg38UCSC Ensembl
OuterchrX:44297214..44305706hg19UCSC Ensembl
OuterchrX:44182158..44190650hg18UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg388493
hg198493
hg188493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565410
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv990696
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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