A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953408



Internal ID17302282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:43304752..43311551hg38UCSC Ensembl
OuterchrX:43164001..43170800hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg386800
hg196800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000880
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953408
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer