A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1331



Internal ID15544387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:85402104..85414069hg38UCSC Ensembl
Outerchr16:85435710..85447675hg19UCSC Ensembl
Outerchr16:83993211..84005176hg18UCSC Ensembl
Outerchr16:83993211..84005176hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3811966
hg1911966
hg1811966
hg1711966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1913
Supporting Variants
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)nssv1331
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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