A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757390



Internal ID18384950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:15355379..15366249hg38UCSC Ensembl
OuterchrX:15353379..15366878hg38UCSC Ensembl
InnerchrX:15373501..15384371hg19UCSC Ensembl
OuterchrX:15371501..15385000hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3813500
hg1913500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558643
Supporting Variants
Samples
Known GenesFIGF, PIR-FIGF
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757390
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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