A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5275



Internal ID15196894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:154346813..154424073hg38UCSC Ensembl
OuterchrX:153575181..153652415hg19UCSC Ensembl
OuterchrX:153228375..153305609hg18UCSC Ensembl
OuterchrX:153096028..153173262hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3877261
hg1977235
hg1877235
hg1777235
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7468
Supporting Variants
SamplesNA19129
Known GenesDNASE1L1, EMD, FLNA, RPL10, SNORA70, TAZ
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)nssv5275
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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