A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3558854



Internal ID18413244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:47403992..47405183hg38UCSC Ensembl
OuterchrX:47403977..47405200hg38UCSC Ensembl
InnerchrX:47263391..47264582hg19UCSC Ensembl
OuterchrX:47263376..47264599hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg381224
hg191224
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9757601
Samples
Known GenesZNF157
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3558854
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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