A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1725



Internal ID15546288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:5986687..6009759hg38UCSC Ensembl
Outerchr16:6036688..6059760hg19UCSC Ensembl
Outerchr16:5976689..5999761hg18UCSC Ensembl
Outerchr16:5976689..5999761hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3823073
hg1923073
hg1823073
hg1723073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7229
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)nsv1725
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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