A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1838



Internal ID15194436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:51700364..51738437hg38UCSC Ensembl
OuterchrX:51438599..51481533hg19UCSC Ensembl
OuterchrX:51455339..51498273hg18UCSC Ensembl
OuterchrX:51271635..51314569hg17UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3838074
hg1942935
hg1842935
hg1742935
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
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)nssv1838
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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