A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1135



Internal ID15545698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:95948379..95981182hg38UCSC Ensembl
Outerchr13:96600633..96633436hg19UCSC Ensembl
Outerchr13:95398634..95431437hg18UCSC Ensembl
Outerchr13:95398634..95431437hg17UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg386638
hg196638
hg186638
hg176638
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6573
SamplesNA12156
Known GenesUGGT2
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)nsv1135
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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