A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1849



Internal ID15541132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:90266234..90290948hg38UCSC Ensembl
OuterchrX:89521233..89545947hg19UCSC Ensembl
OuterchrX:89407889..89432603hg18UCSC Ensembl
OuterchrX:89327378..89352092hg17UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg389627
hg199627
hg189627
hg179627
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6991
Supporting Variants
SamplesNA18555
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)nssv1849
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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