A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv850



Internal ID15544858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:11693500..11715218hg38UCSC Ensembl
OuterchrX:11711620..11733338hg19UCSC Ensembl
OuterchrX:11621541..11643259hg18UCSC Ensembl
OuterchrX:11471277..11492995hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3821719
hg1921719
hg1821719
hg1721719
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6799
Supporting Variants
SamplesNA19240
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)nssv850
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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