A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757793



Internal ID18732039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:85088025..85088206hg38UCSC Ensembl
OuterchrX:85087976..85088237hg38UCSC Ensembl
InnerchrX:84343031..84343212hg19UCSC Ensembl
OuterchrX:84342982..84343243hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559046
Supporting Variants
Samples
Known GenesAPOOL
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757793
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer