A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1826



Internal ID15546389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:62480166..62525777hg38UCSC Ensembl
Outerchr16:62514070..62559681hg19UCSC Ensembl
Outerchr16:61071571..61117182hg18UCSC Ensembl
Outerchr16:61071571..61117182hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3845612
hg1945612
hg1845612
hg1745612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5606, nssv4217, nssv6675
SamplesNA12156, NA12878, NA19129
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)nsv1826
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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