A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv938



Internal ID15198366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:154313777..154377485hg38UCSC Ensembl
OuterchrX:153542127..153605845hg19UCSC Ensembl
OuterchrX:153195321..153259039hg18UCSC Ensembl
OuterchrX:153062974..153126692hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3863709
hg1963719
hg1863719
hg1763719
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7468
Supporting Variants
SamplesNA19240
Known GenesFLNA, TKTL1
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)nssv938
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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