A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757353



Internal ID18731599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:9730209..9730377hg38UCSC Ensembl
OuterchrX:9730190..9730396hg38UCSC Ensembl
InnerchrX:9698249..9698417hg19UCSC Ensembl
OuterchrX:9698230..9698436hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558606
Supporting Variants
Samples
Known GenesGPR143
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757353
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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