A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3559476



Internal ID18760552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:152007279..152007462hg38UCSC Ensembl
OuterchrX:152007272..152007469hg38UCSC Ensembl
InnerchrX:151175751..151175934hg19UCSC Ensembl
OuterchrX:151175744..151175941hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9758223
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3559476
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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