A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6335



Internal ID15190843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:55464236..55547739hg38UCSC Ensembl
OuterchrX:55490669..55574172hg19UCSC Ensembl
OuterchrX:55507394..55590897hg18UCSC Ensembl
OuterchrX:55373690..55457193hg17UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3883504
hg1983504
hg1883504
hg1783504
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7448
Supporting Variants
SamplesNA12156
Known GenesUSP51
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)nssv6335
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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