A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6818



Internal ID15205079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:17407692..17452501hg38UCSC Ensembl
OuterchrX:17425815..17470624hg19UCSC Ensembl
OuterchrX:17335736..17380545hg18UCSC Ensembl
OuterchrX:17185472..17230281hg17UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg3844810
hg1944810
hg1844810
hg1744810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8693
SamplesNA12156
Known GenesMIR4768, NHS
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)nsv6818
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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