A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10729



Internal ID15195383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:120023559..120173068hg38UCSC Ensembl
OuterchrX:119157524..119306923hg19UCSC Ensembl
OuterchrX:119041552..119190951hg18UCSC Ensembl
OuterchrX:118939406..119088805hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38149510
hg19149400
hg18149400
hg17149400
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)nssv10729
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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