A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11232



Internal ID15192661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:154358105..154413258hg38UCSC Ensembl
OuterchrX:153586473..153641595hg19UCSC Ensembl
OuterchrX:153239667..153294789hg18UCSC Ensembl
OuterchrX:153107320..153162442hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3855154
hg1955123
hg1855123
hg1755123
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7468
Supporting Variants
SamplesNA15510
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)nssv11232
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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