A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757949



Internal ID18732195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:114027963..114074701hg38UCSC Ensembl
OuterchrX:114020988..114079302hg38UCSC Ensembl
InnerchrX:113271151..113317891hg19UCSC Ensembl
OuterchrX:113264216..113322500hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3858315
hg1958285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559202
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757949
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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