A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1900



Internal ID15199777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:81752035..81783699hg38UCSC Ensembl
Outerchr16:81785640..81817304hg19UCSC Ensembl
Outerchr16:80343141..80374805hg18UCSC Ensembl
Outerchr16:80343141..80374805hg17UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg387765
hg197765
hg187765
hg177765
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6687
SamplesNA12156
Known GenesPLCG2
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)nsv1900
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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