A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757851



Internal ID18732097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:93990056..93993001hg38UCSC Ensembl
OuterchrX:93990002..93993382hg38UCSC Ensembl
InnerchrX:93245055..93248000hg19UCSC Ensembl
OuterchrX:93245001..93248381hg19UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg383381
hg193381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559104
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757851
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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