A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6815



Internal ID15205076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:16609172..16640869hg38UCSC Ensembl
OuterchrX:16627295..16658992hg19UCSC Ensembl
OuterchrX:16537216..16568913hg18UCSC Ensembl
OuterchrX:16386952..16418649hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg387718
hg197718
hg187718
hg177718
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6311
SamplesNA12156
Known GenesCTPS2
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)nsv6815
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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