A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7321



Internal ID8519301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:77984360..77993232hg38UCSC Ensembl
Outerchr10:79744118..79752990hg19UCSC Ensembl
Outerchr10:79414124..79422996hg18UCSC Ensembl
Outerchr10:79414124..79422996hg17UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3818937
hg1918937
hg1818937
hg1718937
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9934
SamplesNA18507
Known GenesPOLR3A
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)nsv7321
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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