A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7591



Internal ID15552616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:124840342..124875179hg38UCSC Ensembl
Outerchr10:126528911..126563748hg19UCSC Ensembl
Outerchr10:126518901..126553738hg18UCSC Ensembl
Outerchr10:126518901..126553738hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg384910
hg194910
hg184910
hg174910
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3905
SamplesNA12878
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)nsv7591
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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