A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3559252



Internal ID18760328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:119769399..119769532hg38UCSC Ensembl
OuterchrX:119769398..119769538hg38UCSC Ensembl
InnerchrX:118903362..118903495hg19UCSC Ensembl
OuterchrX:118903361..118903501hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9757999
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3559252
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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