A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6859



Internal ID15551810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:34772818..34818012hg38UCSC Ensembl
OuterchrX:34790935..34836129hg19UCSC Ensembl
OuterchrX:34700856..34746050hg18UCSC Ensembl
OuterchrX:34550592..34595786hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3845195
hg1945195
hg1845195
hg1745195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8707
SamplesNA12156
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)nsv6859
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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