A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1829



Internal ID15541112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:11918444..11948759hg38UCSC Ensembl
OuterchrX:11936563..11966878hg19UCSC Ensembl
OuterchrX:11846484..11876799hg18UCSC Ensembl
OuterchrX:11696220..11726535hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3830316
hg1930316
hg1830316
hg1730316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6800
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)nssv1829
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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