A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6836



Internal ID15205099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:23905541..23938610hg38UCSC Ensembl
OuterchrX:23923658..23956727hg19UCSC Ensembl
OuterchrX:23833579..23866648hg18UCSC Ensembl
OuterchrX:23683315..23716384hg17UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg386367
hg196367
hg186367
hg176367
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8700
SamplesNA12156
Known GenesAPOO, CXorf58
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv6836
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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