A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757232



Internal ID18731478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:1416319..1416385hg38UCSC Ensembl
OuterchrX:1416318..1416388hg38UCSC Ensembl
InnerchrX:1535212..1535278hg19UCSC Ensembl
OuterchrX:1535211..1535281hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558485
Supporting Variants
Samples
Known GenesASMTL
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757232
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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