A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1909



Internal ID15541192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:109810490..109820597hg38UCSC Ensembl
Outerchr10:111570248..111580355hg19UCSC Ensembl
Outerchr10:111560238..111570345hg18UCSC Ensembl
Outerchr10:111560238..111570345hg17UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3810108
hg1910108
hg1810108
hg1710108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7545
Supporting Variants
SamplesNA18555
Known Genes
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)nssv1909
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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