A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1851



Internal ID15194449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:100857971..100890941hg38UCSC Ensembl
OuterchrX:100112960..100145930hg19UCSC Ensembl
OuterchrX:99999616..100032586hg18UCSC Ensembl
OuterchrX:99919105..99952075hg17UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg387043
hg197043
hg187043
hg177043
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7011
Supporting Variants
SamplesNA18555
Known GenesNOX1
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)nssv1851
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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