A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3559009



Internal ID18760085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:79816734..79817010hg38UCSC Ensembl
OuterchrX:79816678..79817058hg38UCSC Ensembl
InnerchrX:79072231..79072507hg19UCSC Ensembl
OuterchrX:79072175..79072555hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38381
hg19381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9757756
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3559009
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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