A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3893



Internal ID15548548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:81941207..81953779hg38UCSC Ensembl
Outerchr3:81990358..82002930hg19UCSC Ensembl
Outerchr3:82073048..82085620hg18UCSC Ensembl
Outerchr3:82073048..82085620hg17UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg385262
hg195262
hg185262
hg175262
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3101, nssv3178
SamplesNA12878, NA18555
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)nsv3893
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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