A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7497



Internal ID15205826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:94974503..95008810hg38UCSC Ensembl
Outerchr10:96734260..96768567hg19UCSC Ensembl
Outerchr10:96724250..96758557hg18UCSC Ensembl
Outerchr10:96724250..96758557hg17UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg385423
hg195423
hg185423
hg175423
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3890
SamplesNA12878
Known GenesCYP2C9
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)nsv7497
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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