A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5276



Internal ID15543578
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 Flag1
Merged StatusS
Merged Variantsnsv7469
Supporting Variants
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)nssv5276
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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