A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5776



Internal ID15550619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:8833059..8867232hg38UCSC Ensembl
Outerchr10:8875022..8909195hg19UCSC Ensembl
Outerchr10:8915028..8949201hg18UCSC Ensembl
Outerchr10:8915028..8949201hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg385570
hg195570
hg185570
hg175570
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3865
SamplesNA12878
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)nsv5776
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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