A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1920



Internal ID15199797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:87990709..88037582hg38UCSC Ensembl
Outerchr16:88024315..88071188hg19UCSC Ensembl
Outerchr16:86581816..86628689hg18UCSC Ensembl
Outerchr16:86581816..86628689hg17UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3846874
hg1946874
hg1846874
hg1746874
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5620
SamplesNA19129
Known GenesBANP
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)nsv1920
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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