A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1828



Internal ID15541111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:11703499..11732963hg38UCSC Ensembl
OuterchrX:11721619..11751082hg19UCSC Ensembl
OuterchrX:11631540..11661003hg18UCSC Ensembl
OuterchrX:11481276..11510739hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3829465
hg1929464
hg1829464
hg1729464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6799
Supporting Variants
SamplesNA18555
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)nssv1828
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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