A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1101



Internal ID15545664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:81017628..81047532hg38UCSC Ensembl
Outerchr13:81591763..81621667hg19UCSC Ensembl
Outerchr13:80489764..80519668hg18UCSC Ensembl
Outerchr13:80489764..80519668hg17UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3811086
hg1911086
hg1811086
hg1711086
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155
SamplesNA19240
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)nsv1101
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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