A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5256



Internal ID15197039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:120036150..120162507hg38UCSC Ensembl
OuterchrX:119170115..119296413hg19UCSC Ensembl
OuterchrX:119054143..119180441hg18UCSC Ensembl
OuterchrX:118951997..119078295hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38126358
hg19126299
hg18126299
hg17126299
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7457
Supporting Variants
SamplesNA19129
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)nssv5256
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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