A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9786



Internal ID15193156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:154354649..154416288hg38UCSC Ensembl
OuterchrX:153583017..153644627hg19UCSC Ensembl
OuterchrX:153236211..153297821hg18UCSC Ensembl
OuterchrX:153103864..153165474hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3861640
hg1961611
hg1861611
hg1761611
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7468
Supporting Variants
SamplesNA18507
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)nssv9786
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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