A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1786



Internal ID15546349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:31624666..31657521hg38UCSC Ensembl
Outerchr16:31635987..31668842hg19UCSC Ensembl
Outerchr16:31543488..31576343hg18UCSC Ensembl
Outerchr16:31543488..31576343hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg386583
hg196583
hg186583
hg176583
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6667
SamplesNA12156
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)nsv1786
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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