A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7570



Internal ID15552593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:119525550..119550957hg38UCSC Ensembl
Outerchr10:121285062..121310469hg19UCSC Ensembl
Outerchr10:121275052..121300459hg18UCSC Ensembl
Outerchr10:121275052..121300459hg17UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg387736
hg197736
hg187736
hg177736
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1911
SamplesNA18555
Known GenesRGS10
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)nsv7570
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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