A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10730



Internal ID15195382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:120052964..120219579hg38UCSC Ensembl
OuterchrX:119186929..119353427hg19UCSC Ensembl
OuterchrX:119070957..119237455hg18UCSC Ensembl
OuterchrX:118968811..119135309hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38166616
hg19166499
hg18166499
hg17166499
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7457
Supporting Variants
SamplesNA18956
Known GenesRHOXF1, RHOXF2, RHOXF2B
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)nssv10730
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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