A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3558563



Internal ID18759639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:4578544..4578697hg38UCSC Ensembl
OuterchrX:4578538..4578701hg38UCSC Ensembl
InnerchrX:4496585..4496738hg19UCSC Ensembl
OuterchrX:4496579..4496742hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9757310
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3558563
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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