A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757811



Internal ID18732057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:87647697..87648322hg38UCSC Ensembl
OuterchrX:87647669..87648366hg38UCSC Ensembl
InnerchrX:86902697..86903322hg19UCSC Ensembl
OuterchrX:86902669..86903366hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38698
hg19698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559064
Supporting Variants
Samples
Known GenesKLHL4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757811
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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