A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757395



Internal ID18731641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:16409577..16410002hg38UCSC Ensembl
OuterchrX:16409478..16410108hg38UCSC Ensembl
InnerchrX:16427700..16428125hg19UCSC Ensembl
OuterchrX:16427601..16428231hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38631
hg19631
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558648
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757395
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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