A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3558657



Internal ID18413047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:17502566..17502787hg38UCSC Ensembl
OuterchrX:17502490..17502846hg38UCSC Ensembl
InnerchrX:17520689..17520910hg19UCSC Ensembl
OuterchrX:17520613..17520969hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9757404
Samples
Known GenesNHS
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3558657
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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