A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7444



Internal ID15552454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:51652533..51749766hg38UCSC Ensembl
OuterchrX:51395467..51492862hg19UCSC Ensembl
OuterchrX:51412207..51509602hg18UCSC Ensembl
OuterchrX:51228503..51325898hg17UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3897234
hg1997396
hg1897396
hg1797396
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10708, nssv1838, nssv1837, nssv9483, nssv870, nssv871
SamplesNA18956, NA18555, NA18517, NA19240
Known GenesCENPVP1, CENPVP2, GSPT2
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)nsv7444
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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