A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6132



Internal ID15204325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:26777152..26786593hg38UCSC Ensembl
Outerchr10:27066081..27075522hg19UCSC Ensembl
Outerchr10:27106087..27115528hg18UCSC Ensembl
Outerchr10:27106087..27115528hg17UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg389442
hg199442
hg189442
hg179442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1883
SamplesNA18555
Known GenesABI1
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)nsv6132
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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