A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1713



Internal ID15199590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:3179211..3212512hg38UCSC Ensembl
Outerchr16:3229212..3262512hg19UCSC Ensembl
Outerchr16:3169213..3202513hg18UCSC Ensembl
Outerchr16:3169213..3202513hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg385985
hg195985
hg185985
hg175985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5584
SamplesNA19129
Known GenesOR1F1
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)nsv1713
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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