A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3558901



Internal ID18759977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:57169496..57169550hg38UCSC Ensembl
chrX:57195929..57195983hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9757648
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3558901
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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