A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1922



Internal ID15199799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:88100113..88184145hg38UCSC Ensembl
Outerchr16:88133719..88217751hg19UCSC Ensembl
Outerchr16:86691220..86775252hg18UCSC Ensembl
Outerchr16:86691220..86775252hg17UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3884033
hg1984033
hg1884033
hg1784033
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7292, nssv7293
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)nsv1922
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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