A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1837



Internal ID15194435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:51653698..51700789hg38UCSC Ensembl
OuterchrX:51396632..51443832hg19UCSC Ensembl
OuterchrX:51413372..51460572hg18UCSC Ensembl
OuterchrX:51229668..51276868hg17UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3847092
hg1947201
hg1847201
hg1747201
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7444
Supporting Variants
SamplesNA18555
Known GenesCENPVP1, CENPVP2
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)nssv1837
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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