A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3558873



Internal ID18759949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:51016609..51019005hg38UCSC Ensembl
OuterchrX:51016566..51019221hg38UCSC Ensembl
InnerchrX:50759609..50762005hg19UCSC Ensembl
OuterchrX:50759566..50762221hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg382656
hg192656
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9757620
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3558873
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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