A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9487



Internal ID15540201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:106277800..106326472hg38UCSC Ensembl
OuterchrX:105521016..105569699hg19UCSC Ensembl
OuterchrX:105407672..105456355hg18UCSC Ensembl
OuterchrX:105327161..105375844hg17UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3848673
hg1948684
hg1848684
hg1748684
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7455
Supporting Variants
SamplesNA18517
Known Genes
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)nssv9487
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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