A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1716



Internal ID15199593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:3511573..3544041hg38UCSC Ensembl
Outerchr16:3561573..3594041hg19UCSC Ensembl
Outerchr16:3501574..3534042hg18UCSC Ensembl
Outerchr16:3501574..3534042hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg386964
hg196964
hg186964
hg176964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6657
SamplesNA12156
Known GenesCLUAP1, NLRC3
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)nsv1716
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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