A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6837



Internal ID15551786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:25214522..25243429hg38UCSC Ensembl
OuterchrX:25232639..25261546hg19UCSC Ensembl
OuterchrX:25142560..25171467hg18UCSC Ensembl
OuterchrX:24992296..25021203hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3810330
hg1910330
hg1810330
hg1710330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5205
SamplesNA19129
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)nsv6837
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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