A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1819



Internal ID15546382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:59011181..59040954hg38UCSC Ensembl
Outerchr16:59045085..59074858hg19UCSC Ensembl
Outerchr16:57602586..57632359hg18UCSC Ensembl
Outerchr16:57602586..57632359hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3829774
hg1929774
hg1829774
hg1729774
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7255
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)nsv1819
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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