A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7509



Internal ID15205839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:97557833..97586895hg38UCSC Ensembl
Outerchr10:99317590..99346652hg19UCSC Ensembl
Outerchr10:99307580..99336642hg18UCSC Ensembl
Outerchr10:99307580..99336642hg17UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3810686
hg1910686
hg1810686
hg1710686
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3892
SamplesNA12878
Known GenesANKRD2, HOGA1, UBTD1
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)nsv7509
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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