A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3558497



Internal ID18759573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1610017..1610084hg38UCSC Ensembl
chrX:1728910..1728977hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9757244
Samples
Known GenesASMT
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3558497
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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