A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7133



Internal ID15552112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:144565145..144624303hg38UCSC Ensembl
OuterchrX:143646666..143705824hg19UCSC Ensembl
OuterchrX:143454327..143513468hg18UCSC Ensembl
OuterchrX:143352181..143411322hg17UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg385828
hg195828
hg185828
hg175828
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv924, nssv8797
SamplesNA12156, NA19240
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)nsv7133
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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