A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7469



Internal ID15552481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:154572068..154594360hg38UCSC Ensembl
OuterchrX:153800299..153822623hg19UCSC Ensembl
OuterchrX:153453493..153475817hg18UCSC Ensembl
OuterchrX:153364003..153386327hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3822293
hg1922325
hg1822325
hg1722325
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5276
SamplesNA19129
Known GenesCTAG1A, CTAG1B
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)nsv7469
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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