A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757737



Internal ID18731983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:76627194..76670091hg38UCSC Ensembl
OuterchrX:76627092..76670242hg38UCSC Ensembl
InnerchrX:75847603..75890484hg19UCSC Ensembl
OuterchrX:75847501..75890635hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg3843151
hg1943135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558990
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757737
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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