A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9481



Internal ID15540195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:47744081..47754428hg38UCSC Ensembl
OuterchrX:47603480..47613827hg19UCSC Ensembl
OuterchrX:47488424..47498771hg18UCSC Ensembl
OuterchrX:47359734..47370081hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3827239
hg1927239
hg1827239
hg1727239
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6889
Supporting Variants
SamplesNA18517
Known Genes
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)nssv9481
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