A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1091



Internal ID15545654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:75708256..75753770hg38UCSC Ensembl
Outerchr13:76282392..76327906hg19UCSC Ensembl
Outerchr13:75180393..75225907hg18UCSC Ensembl
Outerchr13:75180393..75225907hg17UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg3845515
hg1945515
hg1845515
hg1745515
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6566
SamplesNA12156
Known GenesLMO7
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)nsv1091
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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