A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3558792



Internal ID18759868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:36725004..36725249hg38UCSC Ensembl
OuterchrX:36724941..36725301hg38UCSC Ensembl
InnerchrX:36743077..36743322hg19UCSC Ensembl
OuterchrX:36743014..36743374hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9757539
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3558792
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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