A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757988



Internal ID18732234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:118920812..118922750hg38UCSC Ensembl
OuterchrX:118920798..118922842hg38UCSC Ensembl
InnerchrX:118054775..118056713hg19UCSC Ensembl
OuterchrX:118054761..118056805hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg382045
hg192045
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559241
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757988
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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