A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1836



Internal ID15546399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:66116149..66149484hg38UCSC Ensembl
Outerchr16:66150052..66183387hg19UCSC Ensembl
Outerchr16:64707553..64740888hg18UCSC Ensembl
Outerchr16:64707553..64740888hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg387653
hg197653
hg187653
hg177653
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1311
SamplesNA19240
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)nsv1836
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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