A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953418



Internal ID17302292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:58537368..58555567hg38UCSC Ensembl
OuterchrX:58563801..58582000hg19UCSC Ensembl
CytobandXp11.1
Allele length
AssemblyAllele length
hg3818200
hg1918200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000889
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953418
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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