A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757320



Internal ID18731566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:5443796..5446265hg38UCSC Ensembl
OuterchrX:5443769..5446281hg38UCSC Ensembl
InnerchrX:5361837..5364306hg19UCSC Ensembl
OuterchrX:5361810..5364322hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg382513
hg192513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558573
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757320
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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