A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1838



Internal ID15199715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:66420117..66453805hg38UCSC Ensembl
Outerchr16:66454020..66487708hg19UCSC Ensembl
Outerchr16:65011521..65045209hg18UCSC Ensembl
Outerchr16:65011521..65045209hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg385747
hg195747
hg185747
hg175747
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7261
SamplesNA12156
Known GenesBEAN1
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)nsv1838
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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