A curated catalogue of human genomic structural variation




Variant Details

Variant: esv988664



Internal ID7075820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:65850924..65861348hg38UCSC Ensembl
OuterchrX:65070766..65081190hg19UCSC Ensembl
OuterchrX:64987491..64997915hg18UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg3810425
hg1910425
hg1810425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565031
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv988664
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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