A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7574



Internal ID15552597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:120934889..120968489hg38UCSC Ensembl
Outerchr10:122694401..122728002hg19UCSC Ensembl
Outerchr10:122684391..122717992hg18UCSC Ensembl
Outerchr10:122684391..122717992hg17UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg385832
hg195832
hg185832
hg175832
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8853
SamplesNA12156
Known GenesMIR5694
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)nsv7574
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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