A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6326



Internal ID15537537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:48347483..48411524hg38UCSC Ensembl
OuterchrX:48206918..48270969hg19UCSC Ensembl
OuterchrX:48091862..48155913hg18UCSC Ensembl
OuterchrX:47963172..48027223hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3864042
hg1964052
hg1864052
hg1764052
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7441
Supporting Variants
SamplesNA12156
Known GenesSSX3, SSX4, SSX4B
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)nssv6326
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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