A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9758006



Internal ID18732252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:120509505..120509759hg38UCSC Ensembl
OuterchrX:120509408..120509829hg38UCSC Ensembl
InnerchrX:119643360..119643614hg19UCSC Ensembl
OuterchrX:119643263..119643684hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38422
hg19422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559259
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9758006
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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