A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757620



Internal ID18731866
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 StatusS
Merged Variantsesv3558873
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757620
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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