A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3558797



Internal ID18759873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:38725247..38728746hg38UCSC Ensembl
OuterchrX:38724247..38729472hg38UCSC Ensembl
InnerchrX:38584501..38588000hg19UCSC Ensembl
OuterchrX:38583501..38588726hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg385226
hg195226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9757544
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3558797
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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