A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7310



Internal ID8519289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:77962983..78007707hg38UCSC Ensembl
Outerchr10:79722741..79767465hg19UCSC Ensembl
Outerchr10:79392747..79437471hg18UCSC Ensembl
Outerchr10:79392747..79437471hg17UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3844725
hg1944725
hg1844725
hg1744725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8820
SamplesNA12156
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)nsv7310
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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